Description: Quantitative competitive ELISA kit for measuring Dog Immunoglobulin G (IgG) in samples from serum, plasma. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Dog Immunoglobulin G (IgG) in serum, plasma and other biological fluids.
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Dog Immunoglobulin G (IgG) in serum, plasma and other biological fluids.
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Dog Immunoglobulin G (IgG) in serum, plasma and other biological fluids.
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Dog Immunoglobulin G (IgG) in serum, plasma and other biological fluids.
Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of Dog Immunoglobulin G (IgG) in samples from Serum, plasma and other biological fluids. with no significant corss-reactivity with analogues from other species.
Description: A competitive ELISA for quantitative measurement of Canine Immunoglobulin G(IgG) in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: A competitive ELISA for quantitative measurement of Canine Immunoglobulin G(IgG) in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: A competitive ELISA for quantitative measurement of Canine Immunoglobulin G(IgG) in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: A competitive Inhibition ELISA kit for detection of Immunoglobulin G from Dog in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
Description: This is Competitive Chemiluminescent immunoassay for detection of Dog Immunoglobulin G (IgG) in serum, plasma and other biological fluids.
Description: This is Competitive Chemiluminescent immunoassay for detection of Dog Immunoglobulin G (IgG) in serum, plasma and other biological fluids.
Description: This is Competitive Chemiluminescent immunoassay for detection of Dog Immunoglobulin G (IgG) in serum, plasma and other biological fluids.
Description: This is Competitive Chemiluminescent immunoassay for detection of Dog Immunoglobulin G (IgG) in serum, plasma and other biological fluids.
Description: A competitive ELISA for quantitative measurement of Canine Immunoglobulin G in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: A competitive ELISA for quantitative measurement of Canine Immunoglobulin G in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: A competitive ELISA for quantitative measurement of Canine Immunoglobulin G in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.
Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Pig IgG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Pig IgG. 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 Pig IgG in the samples is then determined by comparing the OD of the samples to the standard curve.
Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Pig IgG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Pig IgG. 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 Pig IgG in the samples is then determined by comparing the OD of the samples to the standard curve.
Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat IgG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat IgG. 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 Rat IgG in the samples is then determined by comparing the OD of the samples to the standard curve.
Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat IgG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat IgG. 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 Rat IgG in the samples is then determined by comparing the OD of the samples to the standard curve.
