人丝氨酸/苏氨酸蛋白激酶LATS2(LATS2)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 LATS2(Serine\/threonine-protein kinase LATS2) ELISA Kit","alternative_names":"LATS2,Serine\/threonine-protein kinase LATS2,Kinase phosphorylated during mitosis protein,Large tumor suppressor homolog 2,Serine\/threonine-protein kinase kpm,Warts-like kinase,KPM","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 LATS2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LATS2. 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 LATS2, 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 LATS2 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"Q9NRM7","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK10063-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK10063-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK10063",}