This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Dog GT. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Dog GT. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Dog GT in the samples is then determined by comparing the OD of the samples to the standard curve.

P01353

around 3 working days

L 16cm x W 15cm x H 9cm

Metabolic pathway;Endocrinology;Gastroenterology;Hormone metabolism;

2h

Serum, plasma and other biological fluids

15.63-1000 pg/mL

1000 pg/mL

4.9 pg/mL

Competitive Inhibition

Dog