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ELISA Kit Canine

An ELISA Kit Canine is a complete plate-based immunoassay system designed for laboratory research and biomolecular testing. The kit includes coated microplates, capture antibodies, detection antibodies, calibrated standards, colorimetric substrates, and optimized assay buffers to ensure high reproducibility and reliable signal development. This canine ELISA kit supports precise, consistent workflows, accurate quantification, and robust performance in research applications, making it ideal for laboratory assays, protein detection, and analytical studies.
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[Canine Estrone ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to Estrone, During the reaction,Estrone in the sample or standard competes with a fixed amount of biotin-labeled Estrone for sites on a pre-coated Monoclonal antibody specific to Estrone. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of Estrone in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine Estrone ELISA Kit

Canine Estrone ELISA Kit

1,00 €
[Canine 5-HIAA ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to 5-HIAA, During the reaction,5-HIAA in the sample or standard competes with a fixed amount of biotin-labeled 5-HIAA for sites on a pre-coated Monoclonal antibody specific to 5-HIAA. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of 5-HIAA in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine 5-HIAA ELISA Kit

Canine 5-HIAA ELISA Kit

1,00 €
[Canine LT-B4 ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to LT-B4 , During the reaction,LT-B4 in the sample or standard competes with a fixed amount of biotin-labeled LT-B4 for sites on a pre-coated Monoclonal antibody specific to LT-B4 . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of LT-B4 in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine LT-B4 ELISA Kit

Canine LT-B4 ELISA Kit

1,00 €
[Canine cAMP ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to cAMP, During the reaction,cAMP in the sample or standard competes with a fixed amount of biotin-labeled cAMP for sites on a pre-coated Monoclonal antibody specific to cAMP. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of cAMP in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine cAMP ELISA Kit

Canine cAMP ELISA Kit

1,00 €
[Canine 2,3-dinor-TXB2 ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to 2,3-dinor-TXB2 , During the reaction,2,3-dinor-TXB2 in the sample or standard competes with a fixed amount of biotin-labeled 2,3-dinor-TXB2 for sites on a pre-coated Monoclonal antibody specific to 2,3-dinor-TXB2 . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of 2,3-dinor-TXB2 in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine 2,3-dinor-TXB2 ELISA Kit

Canine 2,3-dinor-TXB2 ELISA Kit

1,00 €
[Canine 6-keto-PGF1a ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to 6-keto-PGF1a , During the reaction,6-keto-PGF1a in the sample or standard competes with a fixed amount of biotin-labeled 6-keto-PGF1a for sites on a pre-coated Monoclonal antibody specific to 6-keto-PGF1a . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of 6-keto-PGF1a in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine 6-keto-PGF1a ELISA Kit

Canine 6-keto-PGF1a ELISA Kit

1,00 €
[Canine PGE1 ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to PGE1 , During the reaction,PGE1 in the sample or standard competes with a fixed amount of biotin-labeled PGE1 for sites on a pre-coated Monoclonal antibody specific to PGE1 . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of PGE1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine PGE1 ELISA Kit

Canine PGE1 ELISA Kit

1,00 €
[Canine FMN ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to FMN , During the reaction,FMN in the sample or standard competes with a fixed amount of biotin-labeled FMN for sites on a pre-coated Monoclonal antibody specific to FMN . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of FMN in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine FMN ELISA Kit

Canine FMN ELISA Kit

1,00 €
[Canine NA/NE ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to NA/NE, During the reaction,NA/NE in the sample or standard competes with a fixed amount of biotin-labeled NA/NE for sites on a pre-coated Monoclonal antibody specific to NA/NE. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of NA/NE in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine NA/NE ELISA Kit

Canine NA/NE ELISA Kit

1,00 €
[Canine 3-NT ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to 3-NT , During the reaction,3-NT in the sample or standard competes with a fixed amount of biotin-labeled 3-NT for sites on a pre-coated Monoclonal antibody specific to 3-NT . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of 3-NT in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine 3-NT ELISA Kit

Canine 3-NT ELISA Kit

1,00 €
[Canine 8-epi-PGF2α ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to 8-epi-PGF2α, During the reaction,8-epi-PGF2α in the sample or standard competes with a fixed amount of biotin-labeled 8-epi-PGF2α for sites on a pre-coated Monoclonal antibody specific to 8-epi-PGF2α. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of 8-epi-PGF2α in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine 8-epi-PGF2α ELISA Kit

Canine 8-epi-PGF2α ELISA Kit

1,00 €
[Canine F-E3 ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to F-E3, During the reaction,F-E3 in the sample or standard competes with a fixed amount of biotin-labeled F-E3 for sites on a pre-coated Monoclonal antibody specific to F-E3. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of F-E3 in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine F-E3 ELISA Kit

Canine F-E3 ELISA Kit

1,00 €
[Canine OT ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to OT , During the reaction,OT in the sample or standard competes with a fixed amount of biotin-labeled OT for sites on a pre-coated Monoclonal antibody specific to OT . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of OT in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine OT ELISA Kit

Canine OT ELISA Kit

1,00 €
[Canine 8-OHdG ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to 8-OHdG , During the reaction,8-OHdG in the sample or standard competes with a fixed amount of biotin-labeled 8-OHdG for sites on a pre-coated Monoclonal antibody specific to 8-OHdG . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of 8-OHdG in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine 8-OHdG ELISA Kit

Canine 8-OHdG ELISA Kit

1,00 €
[Canine VC ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to VC, During the reaction,VC in the sample or standard competes with a fixed amount of biotin-labeled VC for sites on a pre-coated Monoclonal antibody specific to VC. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of VC in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine VC ELISA Kit

Canine VC ELISA Kit

1,00 €
[Canine 25-HVD3 ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to 25-HVD3 , During the reaction,25-HVD3 in the sample or standard competes with a fixed amount of biotin-labeled 25-HVD3 for sites on a pre-coated Monoclonal antibody specific to 25-HVD3 . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of 25-HVD3 in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine 25-HVD3 ELISA Kit

Canine 25-HVD3 ELISA Kit

1,00 €
[Canine 5METHF ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to 5METHF, During the reaction,5METHF in the sample or standard competes with a fixed amount of biotin-labeled 5METHF for sites on a pre-coated Monoclonal antibody specific to 5METHF. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of 5METHF in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine 5METHF ELISA Kit

Canine 5METHF ELISA Kit

1,00 €
[Canine GSH ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to GSH , During the reaction,GSH in the sample or standard competes with a fixed amount of biotin-labeled GSH for sites on a pre-coated Monoclonal antibody specific to GSH . Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of GSH in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine GSH ELISA Kit

Canine GSH ELISA Kit

1,00 €
[Canine Oxtc ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to Oxtc, During the reaction,Oxtc in the sample or standard competes with a fixed amount of biotin-labeled Oxtc for sites on a pre-coated Monoclonal antibody specific to Oxtc. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of Oxtc in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine Oxtc ELISA Kit

Canine Oxtc ELISA Kit

1,00 €
[Canine CRO ELISA Kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in th is kit has been pre-coated with an antibody specific to CRO, During the reaction,CRO in the sample or standard competes with a fixed amount of biotin-labeled CRO for sites on a pre-coated Monoclonal antibody specific to CRO. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of CRO in the samples is then determined by comparing the O.D. of the samples to the standard curve.] Canine CRO ELISA Kit

Canine CRO ELISA Kit

1,00 €