人MYC诱导核抗原(MINA)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 MINA(MYC Induced Nuclear Antigen) ELISA Kit","alternative_names":"MDIG; NO52; MINA53; ROX; Mineral dust-induced gene protein; Nucleolar protein 52; 60S ribosomal protein L27a histidine hydroxylase; Ribosomal oxygenase MINA","species":"Human","assay_type":"Sandwich","sensitivity":"0.057 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":"Tumor immunity;","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 MINA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MINA. 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 MINA, 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 MINA in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"Q8IUF8","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK7562-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK7562-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK7562",}