McKesson BioServices

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Rat Immunoglobulin M (IgM) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Rat Immunoglobulin M (IgM) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Rat Immunoglobulin M (IgM) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of Rat Immunoglobulin M (IgM) in serum, plasma and other biological fluids.

Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of Rat Immunoglobulin M (IgM) in samples from serum, plasma and other biological fluids with no significant corss-reactivity with analogues from other species.

Description: Quantitativecompetitive ELISA kit for measuring Rat Immunoglobulin M, IgM in samples from serum, plasma. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.

Description: Rattus norvegicus (Rat)

Description: Quantitativecompetitive ELISA kit for measuring Rat Immunoglobulin M, IgM 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: Rattus norvegicus (Rat)

Description: A sandwich quantitative ELISA assay kit for detection of Rat Immunoglobulin M (IgM) in samples from serum or plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Rat Immunoglobulin M (IgM) in samples from serum or plasma.

Description: Rat (Rattus norvegicus)

Description: Rat (Rattus norvegicus)

Description: Rat

Description: Sandwich ELISA

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Immunoglobulin M (IgM) in serum and plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Immunoglobulin M (IgM) in serum and plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Immunoglobulin M (IgM) in serum and plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Immunoglobulin M (IgM) in serum and plasma.

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

Description: A sandwich ELISA kit for quantitative measurement of Rat IgM (Immunoglobulin M) in samples from Serum, Plasma, Cell supernatant

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

Description: A competitive Inhibition ELISA kit for detection of Immunoglobulin M from Rat in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Description: 4.69 ng/mL

Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Goat;Sensitivity: 0.141 ng/ml

Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Mus ;Sensitivity: 0.188 ng/ml

Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Sheep;Sensitivity: 0.469 ng/ml

Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse IgM protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse IgM. 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 Mouse IgM 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 Mouse IgM protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse IgM. 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 Mouse IgM 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 IgM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IgM. 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 IgM, 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 IgM 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 IgM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IgM. 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 IgM, 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 IgM in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Homo sapiens;Sensitivity: 1.875 ng/ml