Anti-Chloride Intracellular Channel Protein 1 Antibody (Anti-CLIC1) BioAssay™ ELISA Kit (Human)

The BioAssay™kit is a enzyme immunoassay for in vitro quantitative measurement of Anti-CLIC1 in human serum, plasma and other biological fluids.||Detection Range:|31.2-2,000pg/ml||Sensitivity:|12.1pg/ml||Specificity:|This assay has high sensitivity and excellent specificity for detection of Anti-Chloride Intracellular Channel Protein 1 Antibody (Anti-CLIC1). No significant cross-reactivity or interference between Anti-Chloride Intracellular Channel Protein 1 Antibody (Anti-CLIC1) and analogues was observed.||Precision:|Intra-Assay %CV: <10%|Inter-Assay %CV: <12%||Test Principle:|The microtiter plate provided in this kit has been pre-coated with CLIC1. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-CLIC1 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 Anti-CLIC1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.||Kit Components:|Pre-coated, ready to use 96-well strip plate|Standard, 2x vials|Detection Reagent A, 1x120ul|Detection Reagent B, 1x120ul|TMB Substrate, 1x9ml|Wash Buffer (30X): 1x20ml|Standard Diluent, 1x20ml|Assay Diluent A, 1x12ml|Assay Diluent B, 1x12ml|Stop Solution, 1x6ml||Storage and Stability:|Store Microtiter Strips, Standard, Detection Reagents and Positive Control at -20°C. After reconstitution of Positive Control, store at 4°C and use within 5 days. Store all the other components at 4°C. Unused kit is stable for 6 months after receipt. Once kit components are opened, it is highly recommended to use remaining reagents within 1 month provided this is within the expiration date of the kit. For maximum recovery of product, centrifuge the original vials after thawing and prior to removing the cap.||Assay Procedure Summary:|1. Prepare all reagents, samples and standards.|2. Add 100ul standard or sample to each well. Incubate 1 hour at 37°C.|3. Aspirate and add 100ul prepared Detection Reagent A. Incubate 1 hour at 37°C.|4. Aspirate and wash 3 times.|5. Add 100ul prepared Detection Reagent B. Incubate 30 minutes at 37°C.|6. Aspirate and wash 5 times.|7. Add 90ul Substrate Solution. Incubate 10-20 minutes at 37°C.|8. Add 50ul Stop Solution. Read at 450nm immediately.