人不均一核糖核蛋白A2/B1(HNRPA2B1)酶联免疫吸附检测试剂盒

产品介绍

• {"48t":"1820","96t":"2600","96t_5":"11050","name_en":"Human HNRPA2B1(Heterogeneous Nuclear Ribonucleoprotein A2\/B1) ELISA Kit","alternative_names":"hnRNP-A2\/B1; hnRNPA2B1; RA33; HnRNPA2\/B1","species":"Human","assay_type":"Sandwich","sensitivity":"0.058 ng\/mL","standard":"10 ng\/mL","detection_range":"0.16-10 ng\/mL","sample_type":"tissue homogenates, cell lysates and other biological fluids","assay_length":"3.5h","research_area":"Signal transduction;Developmental science;","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 HNRPA2B1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HNRPA2B1. 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 HNRPA2B1, 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 HNRPA2B1 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"P22626","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK1535-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK1535-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK1535",}