人多聚ADP核糖聚合酶4(PARP4)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 PARP4(Poly ADP Ribose Polymerase 4) ELISA Kit","alternative_names":"ADPRTL1; ARTD4; PARPL; PH5P; VAULT3; VPARP; P193; VWA5C; von Willebrand Factor A Domain Containing 5C; ADP-ribosyltransferase diphtheria toxin-like 4; Vault polymerase","species":"Human","assay_type":"Sandwich","sensitivity":"0.063 ng\/mL","standard":"10 ng\/mL","detection_range":"0.16-10 ng\/mL","sample_type":"Tissue homogenates and other biological fluids.","assay_length":"3.5h","research_area":"Enzyme & Kinase;","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 PARP4. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PARP4. 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 PARP4, 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 PARP4 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"Q9UKK3","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK3564-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK3564-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK3564",}