大鼠CD3分子(CD3)酶联免疫吸附检测试剂盒

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• {"48t":"1960","96t":"2800","96t_5":"11900","name_en":"Rat CD3(Cluster of Differentiation 3) ELISA Kit","alternative_names":"CD3; CD3e antigen; CD3e antigen; epsilon polypeptide; TiT3 complex; CD3e molecule; epsilon; CD3-TCR complex; CD3-epsilon; FLJ18683; T3E; T-cell antigen receptor complex; epsilon subunit of T3; T-cell surface antigen T3; Leu-4 epsilon chain; T-cell surface glycoprotein CD3 epsilon chain; TCRE","species":"Rat","assay_type":"Sandwich","sensitivity":"0.124 ng\/mL","standard":"20 ng\/mL","detection_range":"0.32-20 ng\/mL","sample_type":"Tissue homogenates and other biological fluids.","assay_length":"3.5h","research_area":"Immunology; 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 Rat CD3. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat CD3. 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 CD3, 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 CD3 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"P04235","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK9162-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK9162-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK9162",}