人丝氨酸/苏氨酸蛋白激酶LATS1(LATS1)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 LATS1(Serine\/threonine-protein kinase LATS1) ELISA Kit","alternative_names":"LATS1,Serine\/threonine-protein kinase LATS1,Large tumor suppressor homolog 1,WARTS protein kinase (h-warts),WARTS","species":"Human","assay_type":"Sandwich","sensitivity":"0.095 ng\/mL","standard":"10 ng\/mL","detection_range":"0.16-10 ng\/mL","sample_type":"serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids","assay_length":"3.5h","research_area":"Metabolism,Signal Transduction","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 LATS1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LATS1. 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 LATS1, 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 LATS1 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"O95835","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK10062-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK10062-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK10062",}