人膜金属内肽酶样蛋白1(MMEL1)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 MMEL1(Membrane metallo-endopeptidase-like 1) ELISA Kit","alternative_names":"Membrane metallo-endopeptidase-like 1;MMEL1;MELL1, MMEL2, NEP2;Neprilysin-2 (NEP2; NL2);Neprilysin II (NEPII)","species":"Human","assay_type":"Sandwich","sensitivity":"13.2 pg\/mL","standard":"2000 pg\/mL","detection_range":"31.25-2000 pg\/mL","sample_type":"serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids","assay_length":"3.5h","research_area":"metabolism;","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 MMEL1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MMEL1. 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 MMEL1, 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 MMEL1 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"Q495T6","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK11302-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK11302-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK11302",}