人CD200受体1(CD200R1)微量上样酶联免疫吸附检测试剂盒

产品介绍

• {"48t":"1960","96t":"2800","96t_5":"11900","name_en":"Human CD200R1(CD200 Receptor 1) Microsample ELISA Kit","alternative_names":"OX2R; HCRTR2; CD200R; MOX2R; MOX2 Receptor; Cell surface glycoprotein CD200 receptor 1; CD200 cell surface glycoprotein receptor; Cell surface glycoprotein OX2 receptor 1","species":"Human","assay_type":"Sandwich","sensitivity":"0.38 ng\/mL","standard":"100 ng\/mL","detection_range":"1.56-100 ng\/mL","sample_type":"Serum, plasma, tissue homogenates, cell lysates and other biological fluids","assay_length":"3.5h","research_area":"CD & Adhesion molecule;","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 CD200R1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CD200R1. 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 CD200R1, 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 CD200R1 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"Q8TD46","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK10766MS-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK10766MS-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK10766MS",}