人硫氧还蛋白还原酶1(TrxR1)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 TrxR1(Thioredoxin Reductase 1) ELISA Kit","alternative_names":"TXNRD1; TR1; GRIM12; KDRF; TRXR-1; TXNR; Gene associated with retinoic and interferon-induced mortality 12 protein; KM-102-derived reductase-like factor","species":"Human","assay_type":"Sandwich","sensitivity":"0.056 ng\/mL","standard":"10 ng\/mL","detection_range":"0.16-10 ng\/mL","sample_type":"serum, plasma, tissue homogenates and other biological fluids","assay_length":"3.5h","research_area":"Signal transduction;Enzyme & Kinase;Metabolic pathway;","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 TrxR1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TrxR1. 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 TrxR1, 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 TrxR1 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"Q16881","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK2000-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK2000-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK2000",}