Tested Sample Types

Control catalog number

Sequence(One Letter Code)

Sequence(One Letter Code)

QuicKey Pro Sheep Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Sheep Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep Pg are added to the micro ELISA plate wells. Sheep Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep Pg in samples.No significant cross-reactivity or interference between Sheep Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_pg(progesterone)_elisa_kit-e_osel_s0005

https://789.bio/ea/5C80aP

https://789.bio/eb/0un9u9

https://onlinelibrary.wiley.com/doi/abs/10.1111/rda.14295

https://789.bio/ec/9af9a1

QuicKey Pro Sheep Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Sheep Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep Pg are added to the micro ELISA plate wells. Sheep Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep Pg in samples.No significant cross-reactivity or interference between Sheep Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_pg(progesterone)_elisa_kit-e_osel_s0005

https://789.bio/ea/5C80aP

https://789.bio/eb/0un9u9

https://onlinelibrary.wiley.com/doi/abs/10.1111/rda.14295

https://789.bio/ec/9af9a1

QuicKey Pro Sheep Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Sheep Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep Pg are added to the micro ELISA plate wells. Sheep Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep Pg in samples.No significant cross-reactivity or interference between Sheep Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_pg(progesterone)_elisa_kit-e_osel_s0005

https://789.bio/ea/5C80aP

https://789.bio/eb/0un9u9

https://onlinelibrary.wiley.com/doi/abs/10.1111/rda.14295

https://789.bio/ec/9af9a1

Cell Biology;Signal transduction;Developmental biology

This ELISA kit applies to the in vitro quantitative determination of Sheep E3 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep E3. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep E3 are added to the micro ELISA plate wells. Sheep E3 in samples (or standards) competes with a fixed amount of E3 on the solid phase supporter for sites on the HRP linked detection antibody specific to E3. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep E3 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep E3 in samples.No significant cross-reactivity or interference between Sheep E3 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_e3(estriol)_elisa_kit-e_osel_s0004

https://789.bio/ea/XTWXTG

https://789.bio/eb/nz9q5C

https://789.bio/ec/ffT8SO

Cell Biology;Signal transduction;Developmental biology

This ELISA kit applies to the in vitro quantitative determination of Sheep E3 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep E3. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep E3 are added to the micro ELISA plate wells. Sheep E3 in samples (or standards) competes with a fixed amount of E3 on the solid phase supporter for sites on the HRP linked detection antibody specific to E3. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep E3 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep E3 in samples.No significant cross-reactivity or interference between Sheep E3 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_e3(estriol)_elisa_kit-e_osel_s0004

https://789.bio/ea/XTWXTG

https://789.bio/eb/nz9q5C

https://789.bio/ec/ffT8SO

Cell Biology;Signal transduction;Developmental biology

This ELISA kit applies to the in vitro quantitative determination of Sheep E3 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep E3. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep E3 are added to the micro ELISA plate wells. Sheep E3 in samples (or standards) competes with a fixed amount of E3 on the solid phase supporter for sites on the HRP linked detection antibody specific to E3. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep E3 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep E3 in samples.No significant cross-reactivity or interference between Sheep E3 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_e3(estriol)_elisa_kit-e_osel_s0004

https://789.bio/ea/XTWXTG

https://789.bio/eb/nz9q5C

https://789.bio/ec/ffT8SO

QuicKey Pro Sheep T (Testosterone) ELISA Kit

Signal Transduction;Signal Transduction;Epigenetics and Nuclear Signaling;Developmental Biology

This ELISA kit applies to the in vitro quantitative determination of Sheep T concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep T. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep T are added to the micro ELISA plate wells. Sheep T in samples (or standards) competes with a fixed amount of T on the solid phase supporter for sites on the HRP linked detection antibody specific to T. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep T in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep T in samples.No significant cross-reactivity or interference between Sheep T and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_t(testosterone)_elisa_kit-e_osel_s0003

https://789.bio/ea/y5840S

https://789.bio/eb/GK0ar1

https://789.bio/ec/9S0Wj1

QuicKey Pro Sheep T (Testosterone) ELISA Kit

Signal Transduction;Signal Transduction;Epigenetics and Nuclear Signaling;Developmental Biology

This ELISA kit applies to the in vitro quantitative determination of Sheep T concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep T. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep T are added to the micro ELISA plate wells. Sheep T in samples (or standards) competes with a fixed amount of T on the solid phase supporter for sites on the HRP linked detection antibody specific to T. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep T in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep T in samples.No significant cross-reactivity or interference between Sheep T and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_t(testosterone)_elisa_kit-e_osel_s0003

https://789.bio/ea/y5840S

https://789.bio/eb/GK0ar1

https://789.bio/ec/9S0Wj1

QuicKey Pro Sheep T (Testosterone) ELISA Kit

Signal Transduction;Signal Transduction;Epigenetics and Nuclear Signaling;Developmental Biology

This ELISA kit applies to the in vitro quantitative determination of Sheep T concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep T. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep T are added to the micro ELISA plate wells. Sheep T in samples (or standards) competes with a fixed amount of T on the solid phase supporter for sites on the HRP linked detection antibody specific to T. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep T in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep T in samples.No significant cross-reactivity or interference between Sheep T and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_t(testosterone)_elisa_kit-e_osel_s0003

https://789.bio/ea/y5840S

https://789.bio/eb/GK0ar1

https://789.bio/ec/9S0Wj1

11β;17α;21-Trihydroxypregn-4-ene-3;20-dione;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Sheep Cortisol concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep Cortisol. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep Cortisol are added to the micro ELISA plate wells. Sheep Cortisol in samples (or standards) competes with a fixed amount of Cortisol on the solid phase supporter for sites on the HRP linked detection antibody specific to Cortisol. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep Cortisol in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep Cortisol in samples.No significant cross-reactivity or interference between Sheep Cortisol and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_cortisol_elisa_kit-e_osel_s0002

https://789.bio/ea/a9COiP

https://789.bio/eb/5OOi9G

https://www.sciencedirect.com/science/article/pii/S0031938422000889

https://www.mdpi.com/1564546

https://789.bio/ec/Te5WTK

11β;17α;21-Trihydroxypregn-4-ene-3;20-dione;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Sheep Cortisol concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep Cortisol. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep Cortisol are added to the micro ELISA plate wells. Sheep Cortisol in samples (or standards) competes with a fixed amount of Cortisol on the solid phase supporter for sites on the HRP linked detection antibody specific to Cortisol. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep Cortisol in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep Cortisol in samples.No significant cross-reactivity or interference between Sheep Cortisol and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_cortisol_elisa_kit-e_osel_s0002

https://789.bio/ea/a9COiP

https://789.bio/eb/5OOi9G

https://www.sciencedirect.com/science/article/pii/S0031938422000889

https://www.mdpi.com/1564546

https://789.bio/ec/Te5WTK

11β;17α;21-Trihydroxypregn-4-ene-3;20-dione;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Sheep Cortisol concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep Cortisol. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep Cortisol are added to the micro ELISA plate wells. Sheep Cortisol in samples (or standards) competes with a fixed amount of Cortisol on the solid phase supporter for sites on the HRP linked detection antibody specific to Cortisol. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep Cortisol in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep Cortisol in samples.No significant cross-reactivity or interference between Sheep Cortisol and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_cortisol_elisa_kit-e_osel_s0002

https://789.bio/ea/a9COiP

https://789.bio/eb/5OOi9G

https://www.sciencedirect.com/science/article/pii/S0031938422000889

https://www.mdpi.com/1564546

https://789.bio/ec/Te5WTK

QuicKey Pro Sheep E2 (Estradiol) ELISA Kit

Oestradiol;E2;17β-Estradiol;Estra-1;3;5(10)-triene-3;17β-diol;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Sheep E2 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep E2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep E2 are added to the micro ELISA plate wells. Sheep E2 in samples (or standards) competes with a fixed amount of E2 on the solid phase supporter for sites on the HRP linked detection antibody specific to E2. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep E2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep E2 in samples.No significant cross-reactivity or interference between Sheep E2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_e2(estradiol)_elisa_kit-e_osel_s0001

https://789.bio/ea/9Wrb18

https://789.bio/eb/yTibb9

https://789.bio/ec/rzTSiH

QuicKey Pro Sheep E2 (Estradiol) ELISA Kit

Oestradiol;E2;17β-Estradiol;Estra-1;3;5(10)-triene-3;17β-diol;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Sheep E2 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep E2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep E2 are added to the micro ELISA plate wells. Sheep E2 in samples (or standards) competes with a fixed amount of E2 on the solid phase supporter for sites on the HRP linked detection antibody specific to E2. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep E2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep E2 in samples.No significant cross-reactivity or interference between Sheep E2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_e2(estradiol)_elisa_kit-e_osel_s0001

https://789.bio/ea/9Wrb18

https://789.bio/eb/yTibb9

https://789.bio/ec/rzTSiH

QuicKey Pro Sheep E2 (Estradiol) ELISA Kit

Oestradiol;E2;17β-Estradiol;Estra-1;3;5(10)-triene-3;17β-diol;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Sheep E2 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Sheep E2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Sheep E2 are added to the micro ELISA plate wells. Sheep E2 in samples (or standards) competes with a fixed amount of E2 on the solid phase supporter for sites on the HRP linked detection antibody specific to E2. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Sheep E2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Sheep E2 in samples.No significant cross-reactivity or interference between Sheep E2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_sheep_e2(estradiol)_elisa_kit-e_osel_s0001

https://789.bio/ea/9Wrb18

https://789.bio/eb/yTibb9

https://789.bio/ec/rzTSiH

QuicKey Pro Rabbit Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Rabbit Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit Pg are added to the micro ELISA plate wells. Rabbit Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit Pg in samples.No significant cross-reactivity or interference between Rabbit Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_pg(progesterone)_elisa_kit-e_osel_rb0003

https://789.bio/ea/9qnzfT

https://789.bio/eb/rbzT4G

https://www.mdpi.com/article/10.3390/vetsci10030179

https://789.bio/ec/8W9404

QuicKey Pro Rabbit Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Rabbit Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit Pg are added to the micro ELISA plate wells. Rabbit Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit Pg in samples.No significant cross-reactivity or interference between Rabbit Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_pg(progesterone)_elisa_kit-e_osel_rb0003

https://789.bio/ea/9qnzfT

https://789.bio/eb/rbzT4G

https://www.mdpi.com/article/10.3390/vetsci10030179

https://789.bio/ec/8W9404

QuicKey Pro Rabbit Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Rabbit Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit Pg are added to the micro ELISA plate wells. Rabbit Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit Pg in samples.No significant cross-reactivity or interference between Rabbit Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_pg(progesterone)_elisa_kit-e_osel_rb0003

https://789.bio/ea/9qnzfT

https://789.bio/eb/rbzT4G

https://www.mdpi.com/article/10.3390/vetsci10030179

https://789.bio/ec/8W9404

11β;17α;21-Trihydroxypregn-4-ene-3;20-dione;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Rabbit Cortisol concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit Cortisol. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit Cortisol are added to the micro ELISA plate wells. Rabbit Cortisol in samples (or standards) competes with a fixed amount of Cortisol on the solid phase supporter for sites on the HRP linked detection antibody specific to Cortisol. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit Cortisol in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit Cortisol in samples.No significant cross-reactivity or interference between Rabbit Cortisol and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_cortisol_elisa_kit-e_osel_rb0002

https://789.bio/ea/Oa18SC

https://789.bio/eb/04OqrL

https://789.bio/ec/ezn98O

11β;17α;21-Trihydroxypregn-4-ene-3;20-dione;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Rabbit Cortisol concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit Cortisol. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit Cortisol are added to the micro ELISA plate wells. Rabbit Cortisol in samples (or standards) competes with a fixed amount of Cortisol on the solid phase supporter for sites on the HRP linked detection antibody specific to Cortisol. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit Cortisol in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit Cortisol in samples.No significant cross-reactivity or interference between Rabbit Cortisol and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_cortisol_elisa_kit-e_osel_rb0002

https://789.bio/ea/Oa18SC

https://789.bio/eb/04OqrL

https://789.bio/ec/ezn98O

11β;17α;21-Trihydroxypregn-4-ene-3;20-dione;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Rabbit Cortisol concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit Cortisol. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit Cortisol are added to the micro ELISA plate wells. Rabbit Cortisol in samples (or standards) competes with a fixed amount of Cortisol on the solid phase supporter for sites on the HRP linked detection antibody specific to Cortisol. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit Cortisol in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit Cortisol in samples.No significant cross-reactivity or interference between Rabbit Cortisol and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_cortisol_elisa_kit-e_osel_rb0002

https://789.bio/ea/Oa18SC

https://789.bio/eb/04OqrL

https://789.bio/ec/ezn98O

QuicKey Pro Rabbit E2 (Estradiol) ELISA Kit

Oestradiol;E2;17β-Estradiol;Estra-1;3;5(10)-triene-3;17β-diol;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Rabbit E2 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit E2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit E2 are added to the micro ELISA plate wells. Rabbit E2 in samples (or standards) competes with a fixed amount of E2 on the solid phase supporter for sites on the HRP linked detection antibody specific to E2. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit E2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit E2 in samples.No significant cross-reactivity or interference between Rabbit E2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_e2(estradiol)_elisa_kit-e_osel_rb0001

https://789.bio/ea/H4q1SK

https://789.bio/eb/PS4O4G

https://789.bio/ec/yvLuT0

QuicKey Pro Rabbit E2 (Estradiol) ELISA Kit

Oestradiol;E2;17β-Estradiol;Estra-1;3;5(10)-triene-3;17β-diol;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Rabbit E2 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit E2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit E2 are added to the micro ELISA plate wells. Rabbit E2 in samples (or standards) competes with a fixed amount of E2 on the solid phase supporter for sites on the HRP linked detection antibody specific to E2. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit E2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit E2 in samples.No significant cross-reactivity or interference between Rabbit E2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_e2(estradiol)_elisa_kit-e_osel_rb0001

https://789.bio/ea/H4q1SK

https://789.bio/eb/PS4O4G

https://789.bio/ec/yvLuT0

QuicKey Pro Rabbit E2 (Estradiol) ELISA Kit

Oestradiol;E2;17β-Estradiol;Estra-1;3;5(10)-triene-3;17β-diol;

Cell biology;Metabolism

This ELISA kit applies to the in vitro quantitative determination of Rabbit E2 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rabbit E2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rabbit E2 are added to the micro ELISA plate wells. Rabbit E2 in samples (or standards) competes with a fixed amount of E2 on the solid phase supporter for sites on the HRP linked detection antibody specific to E2. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rabbit E2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rabbit E2 in samples.No significant cross-reactivity or interference between Rabbit E2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rabbit_e2(estradiol)_elisa_kit-e_osel_rb0001

https://789.bio/ea/H4q1SK

https://789.bio/eb/PS4O4G

https://789.bio/ec/yvLuT0

QuicKey Pro Rat PCSK9 (Proprotein convertase subtilisin/kexin type 9) ELISA Kit

FH3;HCHOLA3;LDLCQ1;NARC-1;NARC1;PC9

Signal Transduction;Metabolism;Neuroscience

This ELISA kit applies to the in vitro quantitative determination of Rat PCSK9 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to PCSK9 . Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for PCSK9 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain PCSK9 , biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 24 nm. The OD value is proportional to the concentration of PCSK9 . You can calculate the concentration of PCSK9 in the samples by comparing the OD of the samples to the standard curve.

This kit recognizes PCSK9 in samples.No significant cross-reactivity or interference between PCSK9 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_pcsk9_(proprotein_convertase_subtilisin/kexin_type_9)_elisa_kit-e_osel_r0016

https://789.bio/ea/W8bouJCA

https://789.bio/eb/9yMqY6Pm

https://789.bio/ec/ueaMnfCP

QuicKey Pro Rat PCSK9 (Proprotein convertase subtilisin/kexin type 9) ELISA Kit

FH3;HCHOLA3;LDLCQ1;NARC-1;NARC1;PC9

Signal Transduction;Metabolism;Neuroscience

This ELISA kit applies to the in vitro quantitative determination of Rat PCSK9 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to PCSK9 . Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for PCSK9 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain PCSK9 , biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 24 nm. The OD value is proportional to the concentration of PCSK9 . You can calculate the concentration of PCSK9 in the samples by comparing the OD of the samples to the standard curve.

This kit recognizes PCSK9 in samples.No significant cross-reactivity or interference between PCSK9 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_pcsk9_(proprotein_convertase_subtilisin/kexin_type_9)_elisa_kit-e_osel_r0016

https://789.bio/ea/W8bouJCA

https://789.bio/eb/9yMqY6Pm

https://789.bio/ec/ueaMnfCP

QuicKey Pro Rat PCSK9 (Proprotein convertase subtilisin/kexin type 9) ELISA Kit

FH3;HCHOLA3;LDLCQ1;NARC-1;NARC1;PC9

Signal Transduction;Metabolism;Neuroscience

This ELISA kit applies to the in vitro quantitative determination of Rat PCSK9 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to PCSK9 . Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for PCSK9 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain PCSK9 , biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 24 nm. The OD value is proportional to the concentration of PCSK9 . You can calculate the concentration of PCSK9 in the samples by comparing the OD of the samples to the standard curve.

This kit recognizes PCSK9 in samples.No significant cross-reactivity or interference between PCSK9 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_pcsk9_(proprotein_convertase_subtilisin/kexin_type_9)_elisa_kit-e_osel_r0016

https://789.bio/ea/W8bouJCA

https://789.bio/eb/9yMqY6Pm

https://789.bio/ec/ueaMnfCP

QuicKey Pro Rat LBP (Lipopolysaccharide Binding Protein) ELISA Kit

LPS-Binding Protein;Lipopolysaccharide Binding Protein;Lipopolysaccharide-Binding Protein;BPI Fold Containing Family D;Member 2;BPIFD2

Cell Biology;Immunology;Neuroscience

This ELISA kit applies to the in vitro quantitative determination of Rat LBP concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat LBP. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat LBP are added to the micro ELISA plate wells. Rat LBP in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat LBP.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat LBP. The concentration of Rat LBP in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes LBP in samples.No significant cross-reactivity or interference between LBP and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_lbp_(lipopolysaccharide_binding_protein)_elisa_kit-e_osel_r0015

https://789.bio/ea/SRpWyD

https://789.bio/eb/pDOV5O

https://789.bio/ec/yLtqLC

QuicKey Pro Rat LBP (Lipopolysaccharide Binding Protein) ELISA Kit

LPS-Binding Protein;Lipopolysaccharide Binding Protein;Lipopolysaccharide-Binding Protein;BPI Fold Containing Family D;Member 2;BPIFD2

Cell Biology;Immunology;Neuroscience

This ELISA kit applies to the in vitro quantitative determination of Rat LBP concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat LBP. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat LBP are added to the micro ELISA plate wells. Rat LBP in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat LBP.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat LBP. The concentration of Rat LBP in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes LBP in samples.No significant cross-reactivity or interference between LBP and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_lbp_(lipopolysaccharide_binding_protein)_elisa_kit-e_osel_r0015

https://789.bio/ea/SRpWyD

https://789.bio/eb/pDOV5O

https://789.bio/ec/yLtqLC

QuicKey Pro Rat LBP (Lipopolysaccharide Binding Protein) ELISA Kit

LPS-Binding Protein;Lipopolysaccharide Binding Protein;Lipopolysaccharide-Binding Protein;BPI Fold Containing Family D;Member 2;BPIFD2

Cell Biology;Immunology;Neuroscience

This ELISA kit applies to the in vitro quantitative determination of Rat LBP concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat LBP. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat LBP are added to the micro ELISA plate wells. Rat LBP in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat LBP.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat LBP. The concentration of Rat LBP in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes LBP in samples.No significant cross-reactivity or interference between LBP and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_lbp_(lipopolysaccharide_binding_protein)_elisa_kit-e_osel_r0015

https://789.bio/ea/SRpWyD

https://789.bio/eb/pDOV5O

https://789.bio/ec/yLtqLC

QuicKey Pro Rat VCAM-1/CD106 (Vascular Cell Adhesion Molecule 1) ELISA Kit

Cancer;Cardiovascular;Neuroscience;Signal transduction

This ELISA kit applies to the in vitro quantitative determination of Rat VCAM-1/CD106 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat VCAM-1/CD106. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat VCAM-1/CD106 are added to the micro ELISA plate wells. Rat VCAM-1/CD106 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat VCAM-1/CD106.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat VCAM-1/CD106. The concentration of Rat VCAM-1/CD106 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes VCAM-1 in samples.No significant cross-reactivity or interference between VCAM-1 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_vcam_1/cd106_(vascular_cell_adhesion_molecule_1)_elisa_kit-e_osel_r0014

https://789.bio/ea/aa1xD0

https://789.bio/eb/PdPGx9

https://789.bio/ec/mu5GRO

QuicKey Pro Rat VCAM-1/CD106 (Vascular Cell Adhesion Molecule 1) ELISA Kit

Cancer;Cardiovascular;Neuroscience;Signal transduction

This ELISA kit applies to the in vitro quantitative determination of Rat VCAM-1/CD106 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat VCAM-1/CD106. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat VCAM-1/CD106 are added to the micro ELISA plate wells. Rat VCAM-1/CD106 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat VCAM-1/CD106.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat VCAM-1/CD106. The concentration of Rat VCAM-1/CD106 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes VCAM-1 in samples.No significant cross-reactivity or interference between VCAM-1 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_vcam_1/cd106_(vascular_cell_adhesion_molecule_1)_elisa_kit-e_osel_r0014

https://789.bio/ea/aa1xD0

https://789.bio/eb/PdPGx9

https://789.bio/ec/mu5GRO

QuicKey Pro Rat VCAM-1/CD106 (Vascular Cell Adhesion Molecule 1) ELISA Kit

Cancer;Cardiovascular;Neuroscience;Signal transduction

This ELISA kit applies to the in vitro quantitative determination of Rat VCAM-1/CD106 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat VCAM-1/CD106. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat VCAM-1/CD106 are added to the micro ELISA plate wells. Rat VCAM-1/CD106 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat VCAM-1/CD106.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat VCAM-1/CD106. The concentration of Rat VCAM-1/CD106 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes VCAM-1 in samples.No significant cross-reactivity or interference between VCAM-1 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_vcam_1/cd106_(vascular_cell_adhesion_molecule_1)_elisa_kit-e_osel_r0014

https://789.bio/ea/aa1xD0

https://789.bio/eb/PdPGx9

https://789.bio/ec/mu5GRO

QuicKey Pro Rat ApoH (Apolipoprotein H) ELISA Kit

Apolipoprotein H;APOH;B2G1;B2GP1;BG;Beta-2-glycoprotein I;Apo-H;Anticardiolipin cofactor;Activated protein C-binding protein;

This ELISA kit applies to the in vitro quantitative determination of Rat ApoH concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ApoH. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ApoH are added to the micro ELISA plate wells. Rat ApoH in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ApoH.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat ApoH. The concentration of Rat ApoH in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes ApoH in samples.No significant cross-reactivity or interference between ApoH and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_apoh_(apolipoprotein_h)_elisa_kit-e_osel_r0013

https://789.bio/ea/1O8p1C

https://789.bio/eb/mm1hqD

https://789.bio/ec/OteyD8

QuicKey Pro Rat ApoH (Apolipoprotein H) ELISA Kit

Apolipoprotein H;APOH;B2G1;B2GP1;BG;Beta-2-glycoprotein I;Apo-H;Anticardiolipin cofactor;Activated protein C-binding protein;

This ELISA kit applies to the in vitro quantitative determination of Rat ApoH concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ApoH. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ApoH are added to the micro ELISA plate wells. Rat ApoH in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ApoH.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat ApoH. The concentration of Rat ApoH in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes ApoH in samples.No significant cross-reactivity or interference between ApoH and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_apoh_(apolipoprotein_h)_elisa_kit-e_osel_r0013

https://789.bio/ea/1O8p1C

https://789.bio/eb/mm1hqD

https://789.bio/ec/OteyD8

QuicKey Pro Rat ApoH (Apolipoprotein H) ELISA Kit

Apolipoprotein H;APOH;B2G1;B2GP1;BG;Beta-2-glycoprotein I;Apo-H;Anticardiolipin cofactor;Activated protein C-binding protein;

This ELISA kit applies to the in vitro quantitative determination of Rat ApoH concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ApoH. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ApoH are added to the micro ELISA plate wells. Rat ApoH in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ApoH.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat ApoH. The concentration of Rat ApoH in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes ApoH in samples.No significant cross-reactivity or interference between ApoH and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_apoh_(apolipoprotein_h)_elisa_kit-e_osel_r0013

https://789.bio/ea/1O8p1C

https://789.bio/eb/mm1hqD

https://789.bio/ec/OteyD8

Cancer; Cell Biology; Cardiovascular

This ELISA kit applies to the in vitro quantitative determination of Rat ACE2 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ACE2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ACE2 are added to the micro ELISA plate wells. Rat ACE2 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ACE2.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat ACE2. The concentration of Rat ACE2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes ACE2 in samples.No significant cross-reactivity or interference between ACE2 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://789.bio/ea/4OZ5d1

https://789.bio/eb/KVSliD

https://789.bio/ec/C4KVHR

Cancer; Cell Biology; Cardiovascular

This ELISA kit applies to the in vitro quantitative determination of Rat ACE2 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ACE2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ACE2 are added to the micro ELISA plate wells. Rat ACE2 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ACE2.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat ACE2. The concentration of Rat ACE2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes ACE2 in samples.No significant cross-reactivity or interference between ACE2 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://789.bio/ea/4OZ5d1

https://789.bio/eb/KVSliD

https://789.bio/ec/C4KVHR

Cancer; Cell Biology; Cardiovascular

This ELISA kit applies to the in vitro quantitative determination of Rat ACE2 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ACE2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ACE2 are added to the micro ELISA plate wells. Rat ACE2 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ACE2.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat ACE2. The concentration of Rat ACE2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes ACE2 in samples.No significant cross-reactivity or interference between ACE2 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://789.bio/ea/4OZ5d1

https://789.bio/eb/KVSliD

https://789.bio/ec/C4KVHR

QuicKey Pro Rat SELP (P-Selectin) ELISA Kit

CD62;CD62P;GMP140;GRMP;LECAM3;PADGEM;PSEL

Immunology;Neuroscience;Cell Biology

This ELISA kit applies to the in vitro quantitative determination of Rat SELP concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat SELP. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat SELP are added to the micro ELISA plate wells. Rat SELP in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat SELP.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat SELP. The concentration of Rat SELP in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes SELP in samples.No significant cross-reactivity or interference between SELP and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_selp_(p_selectin)_elisa_kit-e_osel_r0011

https://789.bio/ea/mySCZ1

https://789.bio/eb/Sp5GCK

https://789.bio/ec/yqe5t9

QuicKey Pro Rat SELP (P-Selectin) ELISA Kit

CD62;CD62P;GMP140;GRMP;LECAM3;PADGEM;PSEL

Immunology;Neuroscience;Cell Biology

This ELISA kit applies to the in vitro quantitative determination of Rat SELP concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat SELP. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat SELP are added to the micro ELISA plate wells. Rat SELP in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat SELP.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat SELP. The concentration of Rat SELP in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes SELP in samples.No significant cross-reactivity or interference between SELP and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_selp_(p_selectin)_elisa_kit-e_osel_r0011

https://789.bio/ea/mySCZ1

https://789.bio/eb/Sp5GCK

https://789.bio/ec/yqe5t9

QuicKey Pro Rat SELP (P-Selectin) ELISA Kit

CD62;CD62P;GMP140;GRMP;LECAM3;PADGEM;PSEL

Immunology;Neuroscience;Cell Biology

This ELISA kit applies to the in vitro quantitative determination of Rat SELP concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat SELP. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat SELP are added to the micro ELISA plate wells. Rat SELP in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat SELP.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat SELP. The concentration of Rat SELP in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes SELP in samples.No significant cross-reactivity or interference between SELP and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_selp_(p_selectin)_elisa_kit-e_osel_r0011

https://789.bio/ea/mySCZ1

https://789.bio/eb/Sp5GCK

https://789.bio/ec/yqe5t9

QuicKey Pro Rat TF (Transferrin) ELISA Kit

F3;CD142;TF;TFA;coagulation factor III;tissue factor

Cardiovascular;Signal transduction

This ELISA kit applies to the in vitro quantitative determination of Rat TF concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat TF. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat TF are added to the micro ELISA plate wells. Rat TF in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat TF.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat TF. The concentration of Rat TF in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes TF in samples.No significant cross-reactivity or interference between TF and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_tf_(transferrin)_elisa_kit-e_osel_r0010

https://789.bio/ea/eDZmu9

https://789.bio/eb/04xuL0

https://789.bio/ec/S8Rpy1

QuicKey Pro Rat TF (Transferrin) ELISA Kit

F3;CD142;TF;TFA;coagulation factor III;tissue factor

Cardiovascular;Signal transduction

This ELISA kit applies to the in vitro quantitative determination of Rat TF concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat TF. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat TF are added to the micro ELISA plate wells. Rat TF in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat TF.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat TF. The concentration of Rat TF in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes TF in samples.No significant cross-reactivity or interference between TF and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_tf_(transferrin)_elisa_kit-e_osel_r0010

https://789.bio/ea/eDZmu9

https://789.bio/eb/04xuL0

https://789.bio/ec/S8Rpy1

QuicKey Pro Rat TF (Transferrin) ELISA Kit

F3;CD142;TF;TFA;coagulation factor III;tissue factor

Cardiovascular;Signal transduction

This ELISA kit applies to the in vitro quantitative determination of Rat TF concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat TF. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat TF are added to the micro ELISA plate wells. Rat TF in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat TF.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat TF. The concentration of Rat TF in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes TF in samples.No significant cross-reactivity or interference between TF and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_tf_(transferrin)_elisa_kit-e_osel_r0010

https://789.bio/ea/eDZmu9

https://789.bio/eb/04xuL0

https://789.bio/ec/S8Rpy1

QuicKey Pro Rat KIM-1 (Kidney Injury Molecule 1) ELISA Kit

HAVCR1;HAVCR;HAVCR-1;KIM-1;KIM1;TIM;TIM-1;TIM1;TIMD-1;TIMD1

This ELISA kit applies to the in vitro quantitative determination of Rat KIM-1 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat KIM-1. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat KIM-1 are added to the micro ELISA plate wells. Rat KIM-1 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat KIM-1.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat KIM-1. The concentration of Rat KIM-1 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes KIM-1 in samples.No significant cross-reactivity or interference between KIM-1 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_kim_1_(kidney_injury_molecule_1)_elisa_kit-e_osel_r0009

https://789.bio/ea/GZ98hH

https://789.bio/eb/Kt1lH8

https://789.bio/ec/Op1VH0

QuicKey Pro Rat KIM-1 (Kidney Injury Molecule 1) ELISA Kit

HAVCR1;HAVCR;HAVCR-1;KIM-1;KIM1;TIM;TIM-1;TIM1;TIMD-1;TIMD1

This ELISA kit applies to the in vitro quantitative determination of Rat KIM-1 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat KIM-1. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat KIM-1 are added to the micro ELISA plate wells. Rat KIM-1 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat KIM-1.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat KIM-1. The concentration of Rat KIM-1 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes KIM-1 in samples.No significant cross-reactivity or interference between KIM-1 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_kim_1_(kidney_injury_molecule_1)_elisa_kit-e_osel_r0009

https://789.bio/ea/GZ98hH

https://789.bio/eb/Kt1lH8

https://789.bio/ec/Op1VH0

QuicKey Pro Rat KIM-1 (Kidney Injury Molecule 1) ELISA Kit

HAVCR1;HAVCR;HAVCR-1;KIM-1;KIM1;TIM;TIM-1;TIM1;TIMD-1;TIMD1

This ELISA kit applies to the in vitro quantitative determination of Rat KIM-1 concentrations in serum, plasma and other biological fluids.

Serum, plasma and other biological fluids

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat KIM-1. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat KIM-1 are added to the micro ELISA plate wells. Rat KIM-1 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat KIM-1.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat KIM-1. The concentration of Rat KIM-1 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes KIM-1 in samples.No significant cross-reactivity or interference between KIM-1 and analogues was observed.

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_kim_1_(kidney_injury_molecule_1)_elisa_kit-e_osel_r0009

https://789.bio/ea/GZ98hH

https://789.bio/eb/Kt1lH8

https://789.bio/ec/Op1VH0

IL1R2;CD121b;CDw121b;IL-1R-2;IL-1RT-2;IL-1RT2;IL1R2c;IL1RB;

Cardiovascular;Immunology;Stem cells

This ELISA kit applies to the in vitro quantitative determination of Rat IL-1R2 concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat IL-1R2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat IL-1R2 are added to the micro ELISA plate wells. Rat IL-1R2 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat IL-1R2.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat IL-1R2. The concentration of Rat IL-1R2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat IL-1R2 in samples.No significant cross-reactivity or interference between Rat IL-1R2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://789.bio/ea/140K8C

https://789.bio/eb/qfX580

https://www.nature.com/articles/s41419-022-04533-1

https://789.bio/ec/0GqTeD

IL1R2;CD121b;CDw121b;IL-1R-2;IL-1RT-2;IL-1RT2;IL1R2c;IL1RB;

Cardiovascular;Immunology;Stem cells

This ELISA kit applies to the in vitro quantitative determination of Rat IL-1R2 concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat IL-1R2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat IL-1R2 are added to the micro ELISA plate wells. Rat IL-1R2 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat IL-1R2.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat IL-1R2. The concentration of Rat IL-1R2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat IL-1R2 in samples.No significant cross-reactivity or interference between Rat IL-1R2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://789.bio/ea/140K8C

https://789.bio/eb/qfX580

https://www.nature.com/articles/s41419-022-04533-1

https://789.bio/ec/0GqTeD

IL1R2;CD121b;CDw121b;IL-1R-2;IL-1RT-2;IL-1RT2;IL1R2c;IL1RB;

Cardiovascular;Immunology;Stem cells

This ELISA kit applies to the in vitro quantitative determination of Rat IL-1R2 concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat IL-1R2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat IL-1R2 are added to the micro ELISA plate wells. Rat IL-1R2 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat IL-1R2.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat IL-1R2. The concentration of Rat IL-1R2 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat IL-1R2 in samples.No significant cross-reactivity or interference between Rat IL-1R2 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://789.bio/ea/140K8C

https://789.bio/eb/qfX580

https://www.nature.com/articles/s41419-022-04533-1

https://789.bio/ec/0GqTeD

QuicKey Pro Rat Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Rat Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat Pg are added to the micro ELISA plate wells. Rat Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rat Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat Pg in samples.No significant cross-reactivity or interference between Rat Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_pg(progesterone)_elisa_kit-e_osel_r0007

https://789.bio/ea/0OK4mP

https://789.bio/eb/bHCibL

https://www.sciencedirect.com/science/article/pii/S0144861722002089

https://www.sciencedirect.com/science/article/pii/S026974912300177X

https://www.mdpi.com/2076-3921/11/10/1879

https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8439717/

https://europepmc.org/article/pmc/pmc9520912?javascript_support=no

https://pubs.rsc.org/en/content/articlelanding/2022/fo/d1fo01744f

https://www.sciencedirect.com/science/article/pii/S0009279723000662

https://www.sciencedirect.com/science/article/pii/S0300483X22002633

https://www.sciencedirect.com/science/article/pii/S0147651320306047

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734354/

https://www.mdpi.com/1134966

https://academic.oup.com/biolreprod/advance-article-abstract/doi/10.1093/biolre/ioac192/6794001

https://789.bio/ec/nDe1i5

QuicKey Pro Rat Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Rat Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat Pg are added to the micro ELISA plate wells. Rat Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rat Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat Pg in samples.No significant cross-reactivity or interference between Rat Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_pg(progesterone)_elisa_kit-e_osel_r0007

https://789.bio/ea/0OK4mP

https://789.bio/eb/bHCibL

https://www.sciencedirect.com/science/article/pii/S0144861722002089

https://www.sciencedirect.com/science/article/pii/S026974912300177X

https://www.mdpi.com/2076-3921/11/10/1879

https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8439717/

https://europepmc.org/article/pmc/pmc9520912?javascript_support=no

https://pubs.rsc.org/en/content/articlelanding/2022/fo/d1fo01744f

https://www.sciencedirect.com/science/article/pii/S0009279723000662

https://www.sciencedirect.com/science/article/pii/S0300483X22002633

https://www.sciencedirect.com/science/article/pii/S0147651320306047

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734354/

https://www.mdpi.com/1134966

https://academic.oup.com/biolreprod/advance-article-abstract/doi/10.1093/biolre/ioac192/6794001

https://789.bio/ec/nDe1i5

QuicKey Pro Rat Pg (Progesterone) ELISA Kit

This ELISA kit applies to the in vitro quantitative determination of Rat Pg concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat Pg. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat Pg are added to the micro ELISA plate wells. Rat Pg in samples (or standards) competes with a fixed amount of Pg on the solid phase supporter for sites on the HRP linked detection antibody specific to Pg. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rat Pg in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat Pg in samples.No significant cross-reactivity or interference between Rat Pg and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_pg(progesterone)_elisa_kit-e_osel_r0007

https://789.bio/ea/0OK4mP

https://789.bio/eb/bHCibL

https://www.sciencedirect.com/science/article/pii/S0144861722002089

https://www.sciencedirect.com/science/article/pii/S026974912300177X

https://www.mdpi.com/2076-3921/11/10/1879

https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8439717/

https://europepmc.org/article/pmc/pmc9520912?javascript_support=no

https://pubs.rsc.org/en/content/articlelanding/2022/fo/d1fo01744f

https://www.sciencedirect.com/science/article/pii/S0009279723000662

https://www.sciencedirect.com/science/article/pii/S0300483X22002633

https://www.sciencedirect.com/science/article/pii/S0147651320306047

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734354/

https://www.mdpi.com/1134966

https://academic.oup.com/biolreprod/advance-article-abstract/doi/10.1093/biolre/ioac192/6794001

https://789.bio/ec/nDe1i5

QuicKey Pro Rat ADP/Acrp30 (Adiponectin) ELISA Kit

Adiponectin;GBP28;ACDC;APM1;ADPN;AdipoQ;ADIPQTL1;

Cancer;Cardiovascular;Metabolism;Neuroscience;Signal transduction;Stem cells

This ELISA kit applies to the in vitro quantitative determination of Rat ADP/Acrp30 concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ADP/Acrp30. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ADP/Acrp30 are added to the micro ELISA plate wells. Rat ADP/Acrp30 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ADP/Acrp30.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat ADP/Acrp30. The concentration of Rat ADP/Acrp30 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat ADP/Acrp30 in samples.No significant cross-reactivity or interference between Rat ADP/Acrp30 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_adp/acrp30(adiponectin)_elisa_kit-e_osel_r0006

https://789.bio/ea/O4ev5C

https://789.bio/eb/Tuzrn1

https://www.mdpi.com/1999-4923/14/7/1368

https://www.mdpi.com/1871912

https://www.mdpi.com/1414304

https://www.mdpi.com/989394

https://www.mdpi.com/2076-3921/9/11/1073

https://www.mdpi.com/1422-0067/22/10/5400

https://pubmed.ncbi.nlm.nih.gov/34305591/

https://www.frontiersin.org/articles/10.3389/fcimb.2021.740236/full

https://www.sciencedirect.com/science/article/pii/S0960076022001303

https://www.sciencedirect.com/science/article/pii/S0899900722003264

https://www.mdpi.com/2131052

https://www.sciencedirect.com/science/article/pii/S0955286320304903

https://789.bio/ec/iDCmnT

QuicKey Pro Rat ADP/Acrp30 (Adiponectin) ELISA Kit

Adiponectin;GBP28;ACDC;APM1;ADPN;AdipoQ;ADIPQTL1;

Cancer;Cardiovascular;Metabolism;Neuroscience;Signal transduction;Stem cells

This ELISA kit applies to the in vitro quantitative determination of Rat ADP/Acrp30 concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ADP/Acrp30. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ADP/Acrp30 are added to the micro ELISA plate wells. Rat ADP/Acrp30 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ADP/Acrp30.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat ADP/Acrp30. The concentration of Rat ADP/Acrp30 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat ADP/Acrp30 in samples.No significant cross-reactivity or interference between Rat ADP/Acrp30 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_adp/acrp30(adiponectin)_elisa_kit-e_osel_r0006

https://789.bio/ea/O4ev5C

https://789.bio/eb/Tuzrn1

https://www.mdpi.com/1999-4923/14/7/1368

https://www.mdpi.com/1871912

https://www.mdpi.com/1414304

https://www.mdpi.com/989394

https://www.mdpi.com/2076-3921/9/11/1073

https://www.mdpi.com/1422-0067/22/10/5400

https://pubmed.ncbi.nlm.nih.gov/34305591/

https://www.frontiersin.org/articles/10.3389/fcimb.2021.740236/full

https://www.sciencedirect.com/science/article/pii/S0960076022001303

https://www.sciencedirect.com/science/article/pii/S0899900722003264

https://www.mdpi.com/2131052

https://www.sciencedirect.com/science/article/pii/S0955286320304903

https://789.bio/ec/iDCmnT

QuicKey Pro Rat ADP/Acrp30 (Adiponectin) ELISA Kit

Adiponectin;GBP28;ACDC;APM1;ADPN;AdipoQ;ADIPQTL1;

Cancer;Cardiovascular;Metabolism;Neuroscience;Signal transduction;Stem cells

This ELISA kit applies to the in vitro quantitative determination of Rat ADP/Acrp30 concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ADP/Acrp30. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat ADP/Acrp30 are added to the micro ELISA plate wells. Rat ADP/Acrp30 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat ADP/Acrp30.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat ADP/Acrp30. The concentration of Rat ADP/Acrp30 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat ADP/Acrp30 in samples.No significant cross-reactivity or interference between Rat ADP/Acrp30 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_adp/acrp30(adiponectin)_elisa_kit-e_osel_r0006

https://789.bio/ea/O4ev5C

https://789.bio/eb/Tuzrn1

https://www.mdpi.com/1999-4923/14/7/1368

https://www.mdpi.com/1871912

https://www.mdpi.com/1414304

https://www.mdpi.com/989394

https://www.mdpi.com/2076-3921/9/11/1073

https://www.mdpi.com/1422-0067/22/10/5400

https://pubmed.ncbi.nlm.nih.gov/34305591/

https://www.frontiersin.org/articles/10.3389/fcimb.2021.740236/full

https://www.sciencedirect.com/science/article/pii/S0960076022001303

https://www.sciencedirect.com/science/article/pii/S0899900722003264

https://www.mdpi.com/2131052

https://www.sciencedirect.com/science/article/pii/S0955286320304903

https://789.bio/ec/iDCmnT

QuicKey Pro Rat IgG (Immunoglobulin G) ELISA Kit

Immunoglobulin G;IgG;

This ELISA kit applies to the in vitro quantitative determination of Rat IgG concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat IgG. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat IgG are added to the micro ELISA plate wells. Rat IgG in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat IgG.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat IgG. The concentration of Rat IgG in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat IgG in samples.No significant cross-reactivity or interference between Rat IgG and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_igg(immunoglobulin_g)_elisa_kit-e_osel_r0005

https://789.bio/ea/zTWDyD

https://789.bio/eb/n5yPu1

https://europepmc.org/article/pmc/pmc9461140?javascript_support=no

https://faseb.onlinelibrary.wiley.com/doi/abs/10.1096/fj.201800102RR

https://www.nature.com/articles/srep31771

https://journals.sagepub.com/doi/abs/10.1177/15593258221123672

https://link.springer.com/article/10.1631/jzus.B1800475

https://789.bio/ec/vnvHOK

QuicKey Pro Rat IgG (Immunoglobulin G) ELISA Kit

Immunoglobulin G;IgG;

This ELISA kit applies to the in vitro quantitative determination of Rat IgG concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat IgG. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat IgG are added to the micro ELISA plate wells. Rat IgG in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat IgG.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat IgG. The concentration of Rat IgG in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat IgG in samples.No significant cross-reactivity or interference between Rat IgG and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_igg(immunoglobulin_g)_elisa_kit-e_osel_r0005

https://789.bio/ea/zTWDyD

https://789.bio/eb/n5yPu1

https://europepmc.org/article/pmc/pmc9461140?javascript_support=no

https://faseb.onlinelibrary.wiley.com/doi/abs/10.1096/fj.201800102RR

https://www.nature.com/articles/srep31771

https://journals.sagepub.com/doi/abs/10.1177/15593258221123672

https://link.springer.com/article/10.1631/jzus.B1800475

https://789.bio/ec/vnvHOK

QuicKey Pro Rat IgG (Immunoglobulin G) ELISA Kit

Immunoglobulin G;IgG;

This ELISA kit applies to the in vitro quantitative determination of Rat IgG concentrations in serum, plasma.

Colorimetric method;ELISA;Sandwich

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat IgG. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat IgG are added to the micro ELISA plate wells. Rat IgG in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Rat IgG.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Rat IgG. The concentration of Rat IgG in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat IgG in samples.No significant cross-reactivity or interference between Rat IgG and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_igg(immunoglobulin_g)_elisa_kit-e_osel_r0005

https://789.bio/ea/zTWDyD

https://789.bio/eb/n5yPu1

https://europepmc.org/article/pmc/pmc9461140?javascript_support=no

https://faseb.onlinelibrary.wiley.com/doi/abs/10.1096/fj.201800102RR

https://www.nature.com/articles/srep31771

https://journals.sagepub.com/doi/abs/10.1177/15593258221123672

https://link.springer.com/article/10.1631/jzus.B1800475

https://789.bio/ec/vnvHOK

Cell Biology;Signal transduction;Developmental biology

This ELISA kit applies to the in vitro quantitative determination of Rat E3 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat E3. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat E3 are added to the micro ELISA plate wells. Rat E3 in samples (or standards) competes with a fixed amount of E3 on the solid phase supporter for sites on the HRP linked detection antibody specific to E3. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rat E3 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat E3 in samples.No significant cross-reactivity or interference between Rat E3 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_e3(estriol)_elisa_kit-e_osel_r0004

https://789.bio/ea/5u9WHO

https://789.bio/eb/HCSqLO

https://789.bio/ec/LOuLKO

Cell Biology;Signal transduction;Developmental biology

This ELISA kit applies to the in vitro quantitative determination of Rat E3 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat E3. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat E3 are added to the micro ELISA plate wells. Rat E3 in samples (or standards) competes with a fixed amount of E3 on the solid phase supporter for sites on the HRP linked detection antibody specific to E3. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rat E3 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat E3 in samples.No significant cross-reactivity or interference between Rat E3 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_e3(estriol)_elisa_kit-e_osel_r0004

https://789.bio/ea/5u9WHO

https://789.bio/eb/HCSqLO

https://789.bio/ec/LOuLKO

Cell Biology;Signal transduction;Developmental biology

This ELISA kit applies to the in vitro quantitative determination of Rat E3 concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat E3. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat E3 are added to the micro ELISA plate wells. Rat E3 in samples (or standards) competes with a fixed amount of E3 on the solid phase supporter for sites on the HRP linked detection antibody specific to E3. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rat E3 in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat E3 in samples.No significant cross-reactivity or interference between Rat E3 and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_e3(estriol)_elisa_kit-e_osel_r0004

https://789.bio/ea/5u9WHO

https://789.bio/eb/HCSqLO

https://789.bio/ec/LOuLKO

QuicKey Pro Rat T (Testosterone) ELISA Kit

Signal Transduction;Signal Transduction;Epigenetics and Nuclear Signaling;Developmental Biology

This ELISA kit applies to the in vitro quantitative determination of Rat T concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat T. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat T are added to the micro ELISA plate wells. Rat T in samples (or standards) competes with a fixed amount of T on the solid phase supporter for sites on the HRP linked detection antibody specific to T. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rat T in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat T in samples.No significant cross-reactivity or interference between Rat T and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_t(testosterone)_elisa_kit-e_osel_r0003

https://789.bio/ea/uPaz98

https://789.bio/eb/eX5un9

https://www.sciencedirect.com/science/article/pii/S0144861722002089

https://www.sciencedirect.com/science/article/pii/S004896972100262X

https://www.mdpi.com/2076-3921/11/10/1879

https://www.sciencedirect.com/science/article/pii/S0147651322010892

https://www.hindawi.com/journals/omcl/2022/2113293/

https://www.sciencedirect.com/science/article/pii/S026974911935955X

https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8439717/

https://www.sciencedirect.com/science/article/pii/S0753332222002591

https://www.hindawi.com/journals/omcl/2021/7382900/

https://europepmc.org/article/pmc/pmc9520912?javascript_support=no

https://pubs.rsc.org/en/content/articlelanding/2022/fo/d1fo01744f

https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7993663/

https://789.bio/ec/5qrjvH

QuicKey Pro Rat T (Testosterone) ELISA Kit

Signal Transduction;Signal Transduction;Epigenetics and Nuclear Signaling;Developmental Biology

This ELISA kit applies to the in vitro quantitative determination of Rat T concentrations in serum, plasma.

Colorimetric method;ELISA;Competitive

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Rat T. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Rat T are added to the micro ELISA plate wells. Rat T in samples (or standards) competes with a fixed amount of T on the solid phase supporter for sites on the HRP linked detection antibody specific to T. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Rat T in the samples is then determined by comparing the OD of the samples to the standard curve.

This kit recognizes Rat T in samples.No significant cross-reactivity or interference between Rat T and analogues was observed

Both intra-CV and inter-CV are < 10%.

QuicKey Pro ELISA Kits

https://www.elabscience.com/p-quickey_pro_rat_t(testosterone)_elisa_kit-e_osel_r0003

https://789.bio/ea/uPaz98

https://789.bio/eb/eX5un9