Human FG(Fibrinogen) ELISA Kit

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Human Fibrinogen (FG) in plasma.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Human Fibrinogen (FG) in plasma.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Human Fibrinogen (FG) in plasma.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Human Fibrinogen (FG) in plasma.

Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of Human Fibrinogen (FG) in samples from plasma with no significant corss-reactivity with analogues from other species.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Fibrinogen (FG) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Fibrinogen (FG) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Fibrinogen (FG) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Fibrinogen (FG) in Plasma.

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

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

Description: A sandwich ELISA kit for quantitative measurement of Human FG (Fibrinogen) in samples from Serum, Plasma, Cell supernatant

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

Description: A sandwich ELISA kit for quantitative measurement of Human FG? (Fibrinogen Beta) in samples from Serum, Plasma, Cell supernatant

Description: A sandwich ELISA kit for quantitative measurement of Human FG? (Fibrinogen Alpha) in samples from Serum, Plasma, Cell supernatant

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

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Pig Fibrinogen (FG) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Pig Fibrinogen (FG) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Pig Fibrinogen (FG) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Pig Fibrinogen (FG) in plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Pig Fibrinogen (FG) in samples from plasma with no significant corss-reactivity with analogues from other species.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Fibrinogen (FG) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Fibrinogen (FG) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Fibrinogen (FG) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Fibrinogen (FG) in plasma.

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

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