Mouse carbohydrate antigen 242 (CA242) quantitative detection kit (ELISA) Instructions for use [kit name] mouse carbohydrate antigen 242 (CA242) quantitative detection kit (ELISA) [kit use] quantitative detection of mouse serum, The content of carbohydrate antigen 242 (CA242) in plasma and related liquid samples. [Detection principle] This kit adopts double antibody two-step sandwich enzyme-linked immunosorbent assay (ELISA). Add the standard and the test sample to the transparent enzyme label coated plate pre-coated with mouse carbohydrate antigen 242 (CA242) antibody. After incubation for a sufficient time, wash to remove unbound components, and then add the enzyme label working solution. After sufficient incubation time, wash to remove unbound components. Substrates A and B are added in sequence, and the substrate (TMB) is converted into a blue product catalyzed by horseradish peroxidase (HRP), which turns yellow under the action of an acid. The shade of the color and the carbohydrate antigen in the sample The concentration of 242 (CA242) was positively correlated. The OD value was measured at a wavelength of 450 nm. Based on the OD value of the standard and the sample, the content of mouse carbohydrate antigen 242 (CA242) in the sample was calculated. [Kit composition] 1 enzyme-coated plate 12 wells × 8 strips 7 Developer A solution 6mL 2 Standard: 96 U / ml 0.6mL 8 Developer B solution 6mL 3 20-fold concentrated washing solution 25mL 9 Stop solution 6mL 4 Standard Product diluent 6mL 10 Instructions 1 copy 5 Sample diluent 6mL 11 Sealing film 2 sheets 6 Enzyme label reagent 6mL 12 Sealed bag 1 Remarks: The standard product diluent is diluted sequentially as follows: 96, 48, 24, 12, 6. 3 U / ml [reagents and equipment not needed] 1, 37 ° C incubator 2. Standard microplate reader 3. Precision pipette and disposable pipette tip 4. Distilled water 5. Disposable test tube 6. Absorbent paper [Operation steps] 1. Preparation: Remove the reagent kit from the refrigerator, re-equilibrate at room temperature for 30 minutes. 2. Mixing solution: dilute the 20-fold concentrated washing solution with distilled water to the original one. 3. Add standard products and samples to be tested: take a sufficient number of enzyme-coated plates and fix them to the frame. Set up standard wells, sample wells to be tested and blank control wells, record the positions of each well in the standard wells. Add 50μL of standard product; first add 10μL of sample to be tested, and then add 40μL of sample diluent (that is, the sample is diluted 5 times); blank control well is not added. 4. Incubation: Incubate in a 37 ° C water bath or thermostat for 30 minutes. 5. Wash the plate: discard the liquid, pat dry on the absorbent paper, fill each hole with the washing solution, let stand for 1min, shake off the washing solution, pat dry on the absorbent paper, repeat the washing 4 times (you can also use the washing machine to press Instructions for washing the board). 6. Add enzyme-labeled working solution: add 50μL of enzyme-labeled working solution to each well, without adding blank control wells. 7. Incubation: Repeat operation 4. 8. Wash the board: repeat the operation of 5. 9. Color development: Add 50μL of developer A solution to each well, then add 50μL of developer B solution, and develop color at 37 ° C in the dark for 15min. 10. Termination: Remove the enzyme labeling plate and add 50μL of stop solution to each well to stop the reaction (the color changes from blue to yellow). 11. Determination: Zero the blank holes, and within 15 minutes after termination, measure the absorbance (OD value) of each well with a wavelength of 450 nm. 12. Calculation: According to the concentration of the standard product and the corresponding OD value, calculate the linear regression equation of the standard curve, and then calculate the corresponding sample concentration on the regression equation according to the OD value of the sample. You can also use various application software to Calculation. The final concentration is the actual measured concentration times the dilution factor. [Sample requirements] 1. The sample must not contain sodium azide (NaN3), because sodium azide (NaN3) is an inhibitor of horseradish peroxidase (HRP). 2. The specimen should be extracted as soon as possible after collection. The extraction should be carried out according to relevant literature. The experiment should be carried out as soon as possible after extraction. If the test cannot be performed immediately, the specimen can be stored at -20 ℃, but repeated freezing and thawing should be avoided. 3. The sample should be fully centrifuged, without hemolysis and particles. [Notes] 1. The experiment is carried out in strict accordance with the instructions, and the result of the experiment must be determined by the reading of the microplate reader. 2. If the enzyme-labeled coated board is not used up after opening, it should be put into a sealed bag and added with desiccant immediately. 3. It is recommended that all standards, samples and blank controls be tested in duplicate, and the average value is taken to reduce the experimental error. 4. If the color is too light, the substrate incubation time can be extended properly. 5. In order to avoid cross-contamination, the standard, sample and blank control should be replaced with a tip for each additional one; the common components such as enzyme working solution, sample diluent and substrate should be added by cantilever, and should not touch the microwell ; Do not reuse the sealing film. 6. The kits are used within the warranty period, and different batches of reagents should not be mixed. 7. Substrate B is sensitive to light and avoid prolonged exposure to light. [Summary of operating procedures] Prepare reagents, samples and standards Add the prepared samples and standards, wash the plate 4 times at 37 ° C for 30 minutes, add the enzyme reagent, wash the plate 4 times at 37 ° C for 30 minutes and add the coloring solution A, B, color development at 37 ° C for 15 minutes. Add stop solution and read OD value within 15 minutes. [Detection range] 3-96 U / ml [Specification] 96 servings / box [Storage] 2-8 ° C, protected from light and moisture save. [Validity period] 6 months Shanghai Yuping Biological Technology Co., Ltd. mainly deals with ELISA kits of various brands and grades, with quality assurance and perfect after-sales service. And provide free generation testing. Serving universities and immunology research units. Technicians serve you better.
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