Mouse TAT(Thrombin/Antithrombin Complex) ELISA Kit

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Thrombin/Antithrombin Complex (TAT) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Thrombin/Antithrombin Complex (TAT) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Thrombin/Antithrombin Complex (TAT) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Thrombin/Antithrombin Complex (TAT) in plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Mouse Thrombin/Antithrombin Complex (TAT) in samples from plasma with no significant corss-reactivity with analogues from other species.

Description: A sandwich ELISA kit for quantitative measurement of Mouse TAT (Thrombin/Antithrombin Complex) in samples from Serum, Plasma, Cell supernatant

Description: A sandwich ELISA kit for detection of Thrombin/Antithrombin Complex from Mouse in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat TAT. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat TAT. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat TAT, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Rat TAT in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat TAT. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat TAT. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat TAT, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Rat TAT in the samples is then determined by comparing the OD of the samples to the standard curve.