人趋化因子C-基元配体2(XCL2)微量上样酶联免疫吸附检测试剂盒

产品介绍

• {"48t":"1680","96t":"2400","96t_5":"10200","name_en":"Human XCL2(Chemokine C-Motif Ligand 2) Microsample ELISA Kit","alternative_names":"SCYC2; SCM-1b; Small Inducible Cytokine Subfamily C Member 2; Cytokine SCM-1 beta; C motif chemokine 2; XC chemokine ligand 2","species":"Human","assay_type":"Sandwich","sensitivity":"0.06 ng\/mL","standard":"10 ng\/mL","detection_range":"0.16-10 ng\/mL","sample_type":"Serum, plasma and other biological fluids.","assay_length":"3.5h","research_area":"Cytokine;Signal transduction;Tumor immunity;Infection immunity;Neuro science;","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 XCL2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human XCL2. 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 XCL2, 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 XCL2 in the samples is then determined by comparing the OD of the samples to the standard curve.","uniprot_id":"Q9UBD3","StandardCurveURL":"https:\/\/www.elkbiotech.cn\/upload\/image\/ELISA\/ELK3409MS-b-1.jpg","ManualURL":"https:\/\/www.elkbiotech.cn\/upload\/file\/ELISA\/ELK3409MS-1.pdf","ProductURL":"https:\/\/www.elkbiotech.cn\/pro\/ELK3409MS",}