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ELK Biotechnology
SKU:ELK4799
Human MHCDRb1(Major Histocompatibility Complex Class II DR Beta 1) ELISA Kit
Human MHCDRb1(Major Histocompatibility Complex Class II DR Beta 1) ELISA Kit
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Alternative Names: HLA-DRB1; HLA-DR1B; HLADRb1; HLA Class II Histocompatibility Antigen,DRB1-9 Beta Chain; HLA class II histocompatibility antigen, DRB1-15 beta chain
Assay Type: Sandwich
Sensitivity: 37 pg/mL
standard: 8000 pg/mL
Detection range: 125-8000 pg/mL
Sample type: serum, plasma, tissue homogenates and other biological fluids
Assay length: 3.5h
Research Area: Tumor immunity;Infection immunity;Immune molecule;Immunodeficiency;Autoimmunity;
Test principle: 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 MHCDRb1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MHCDRb1. 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 MHCDRb1, 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 MHCDRb1 in the samples is then determined by comparing the OD of the samples to the standard curve.
UniProt ID: P01911
Assay Type: Sandwich
Sensitivity: 37 pg/mL
standard: 8000 pg/mL
Detection range: 125-8000 pg/mL
Sample type: serum, plasma, tissue homogenates and other biological fluids
Assay length: 3.5h
Research Area: Tumor immunity;Infection immunity;Immune molecule;Immunodeficiency;Autoimmunity;
Test principle: 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 MHCDRb1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MHCDRb1. 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 MHCDRb1, 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 MHCDRb1 in the samples is then determined by comparing the OD of the samples to the standard curve.
UniProt ID: P01911
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