人前列腺素内过氧化物合酶2(PTGS2/COX-2)酶联免疫吸附检测试剂盒

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• {"48t":"1820","96t":"2600","96t_5":"11050","name_en":"Human PTGS2\/COX-2(Prostaglandin Endoperoxide Synthase 2) ELISA Kit","alternative_names":"PGG\/HS; PGHS2; PHS2; HCox2; COX2; Cyclooxygenase 2; Prostaglandin G\/H Synthase And Cyclooxygenase; Prostaglandin H2 synthase 2; PTGS2; Prostaglandin Endoperoxide Synthase 2","species":"Human","assay_type":"Sandwich","sensitivity":"0.125 ng\/mL","standard":"20 ng\/mL","detection_range":"0.32-20 ng\/mL","sample_type":"serum, plasma, tissue homogenates and other biological fluids","assay_length":"3.5h","research_area":"Enzyme & Kinase;Tumor immunity;Infection immunity;Reproductive science;Pulmonology;Gastroenterology;Hormone 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 PTGS2\/COX-2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PTGS2\/COX-2. 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 PTGS2\/COX-2, 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 PTGS2\/COX-2 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"P35354","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK2096-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK2096-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK2096",}