ELISA Reagent

Description: A sandwich ELISA kit for detection of Heparin Cofactor II from Mouse in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Description: plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Mouse Heparin Cofactor II (HCII) in samples from plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Mouse Heparin Cofactor II (HCII) in samples from plasma.

Description: plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Heparin Cofactor II (HCII) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Heparin Cofactor II (HCII) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Heparin Cofactor II (HCII) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Heparin Cofactor II (HCII) in Plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Mouse Heparin Cofactor II (HCII) in samples from Plasma with no significant corss-reactivity with analogues from other species.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

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 HCII. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat HCII. 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 HCII, 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 HCII 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 HCII. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat HCII. 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 HCII, 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 HCII 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 Human HCII. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HCII. 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 Human HCII, 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 Human HCII 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 Human HCII. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HCII. 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 Human HCII, 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 Human HCII 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 Rabbit HCII. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rabbit HCII. 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 Rabbit HCII, 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 Rabbit HCII 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 Rabbit HCII. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rabbit HCII. 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 Rabbit HCII, 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 Rabbit HCII in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Rat Heparin Cofactor II (HCII) in samples from plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Rat Heparin Cofactor II (HCII) in samples from plasma.

Description: plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Heparin Cofactor II (HCII) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Heparin Cofactor II (HCII) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Heparin Cofactor II (HCII) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Heparin Cofactor II (HCII) in Plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Rat Heparin Cofactor II (HCII) in samples from Plasma. with no significant corss-reactivity with analogues from other species.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.