小鼠Ⅱ类主要组织相容性复合体DRβ1(MHCDRb1)酶联免疫吸附检测试剂盒

产品介绍

• {"48t":"1960","96t":"2800","96t_5":"11900","name_en":"Mouse MHCDRb1(Major Histocompatibility Complex Class II DR Beta 1) ELISA Kit","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","species":"Mouse","assay_type":"Sandwich","sensitivity":"12 pg\/mL","standard":"2500 pg\/mL","detection_range":"39.07-2500 pg\/mL","sample_type":"Serum, plasma, tissue homogenates, cell lysates 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 Mouse MHCDRb1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse 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 Mouse 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 Mouse MHCDRb1 in the samples is then determined by comparing the OD of the samples to the standard curve.","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK7247-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK7247-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK7247",}