General SPH(Sphingomyelin) ELISA Kit

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Sphingomyelin (SPH) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Sphingomyelin (SPH) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Sphingomyelin (SPH) in serum, plasma and other biological fluids.

Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Sphingomyelin (SPH) in serum, plasma and other biological fluids.

Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of General Sphingomyelin (SPH) in samples from Serum, plasma and other biological fluids with no significant corss-reactivity with analogues from other species.

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

Description: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with SPH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to SPH. 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 SPH 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 SPH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to SPH. 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 SPH 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