大鼠α1-微球蛋白(a1M)酶联免疫吸附检测试剂盒

产品介绍

• {"48t":"1820","96t":"2600","96t_5":"11050","name_en":"Rat a1M(Alpha-1-Microglobulin\/Bikunin Precursor) ELISA Kit","alternative_names":"AMBP; UTI; HCP; EDC1; HI30; IATIL; ITILC; ITI; ITIL; Alpha 1 Microglobulin\/Bikunin Precursor; Growth-inhibiting protein 19; Uristatin; Uronic-Acid-Rich Protein; Trypstatin","species":"Rat","assay_type":"Sandwich","sensitivity":"0.133 µg\/mL","standard":"20 µg\/mL","detection_range":"0.312-20 µg\/mL","sample_type":"Serum, plasma, urine and other biological fluids","assay_length":"3.5h","research_area":"Infection immunity;Immune molecule;Kidney biomarker;","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 Rat a1M. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat a1M. 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 Rat a1M, 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 Rat a1M in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"Q64240","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK11139-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK11139-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK11139",}