Our ELISA kit quality assurance, excellent quality, affordable, is your first choice for biological experiments, if you need to contact our sales staff. This reagent is for research use only: This kit is used to determine the activity of trypsin in the small intestine of fish. Experimental principle : This kit uses the double antibody sandwich method to determine the level of trypsin in the specimen. The microplate was coated with purified fish trypsin antibody to prepare a solid phase antibody, and trypsin was sequentially added to the microcapsules of the coated monoclonal antibody, and then combined with HRP-labeled trypsin antibody. The antibody-antigen-enzyme-labeled antibody complex was formed, and after thorough washing, the substrate TMB was added for color development. TMB is converted to blue under the catalysis of HRP enzyme and converted to the final yellow color by the action of an acid. The color depth is positively correlated with trypsin in the sample. The absorbance (OD value) was measured with a microplate reader at a wavelength of 450 nm, and the concentration of trypsin in the sample was calculated from a standard curve. Kit composition : Kit composition 48 hole configuration 96-well configuration save Instruction manual 1 copy 1 copy Sealing film 2 pieces (48) 2 pieces (96) sealed bag 1 1 Enzyme label coated plate 1×48 1×96 Store at 2-8 ° C Standard: 360 IU/L 0.5ml × 1 bottle 0.5ml × 1 bottle Store at 2-8 ° C Standard dilution 1.5ml × 1 bottle 1.5ml × 1 bottle Store at 2-8 ° C Enzyme standard reagent 3 ml × 1 bottle 6 ml × 1 bottle Store at 2-8 ° C Sample diluent 3 ml × 1 bottle 6 ml × 1 bottle Store at 2-8 ° C Developer A solution 3 ml × 1 bottle 6 ml × 1 bottle Store at 2-8 ° C Developer B solution 3 ml × 1 bottle 6 ml × 1 bottle Store at 2-8 ° C Stop solution 3ml × 1 bottle 6ml × 1 bottle Store at 2-8 ° C Concentrated washing solution (20ml × 20 times) × 1 bottle (20ml × 30 times) × 1 bottle Store at 2-8 ° C Sample processing and requirements : 1. Serum: The blood is naturally coagulated for 10-20 minutes at room temperature and centrifuged for about 20 minutes (2000-3000 rpm). The supernatant is carefully collected, and if precipitation occurs during storage, it should be centrifuged again. 2. Plasma: EDTA or sodium citrate should be selected as an anticoagulant according to the requirements of the specimen. After mixing for 10-20 minutes, centrifuge for about 20 minutes (2000-3000 rpm). The supernatant is carefully collected, and if a precipitate forms during storage, it should be centrifuged again. 3. Urine: Collect with a sterile tube and centrifuge for about 20 minutes (2000-3000 rpm). The supernatant is carefully collected, and if a precipitate forms during storage, it should be centrifuged again. The chest and ascites and cerebrospinal fluid are referred to. 4. Cell culture supernatant: When detecting secreted components, collect them in a sterile tube. Centrifuge for about 20 minutes (2000-3000 rpm). Collect the supernatant carefully. When the components in the cells were detected, the cell suspension was diluted with PBS (pH 7.2-7.4), and the cell concentration reached about 1 million/ml. By repeated freezing and thawing, the cells are destroyed and the intracellular components are released. Centrifuge for about 20 minutes (2000-3000 rpm). Collect the supernatant carefully. If a precipitate forms during storage, it should be centrifuged again. 5. Tissue specimen: After cutting the specimen, weigh the weight. Add a certain amount of PBS, pH 7.4. It was quickly frozen and stored in liquid nitrogen for use. The specimen still maintains a temperature of 2-8 ° C after melting. A certain amount of PBS (pH 7.4) was added, and the specimen was homogenized by hand or homogenizer. Centrifuge for about 20 minutes (2000-3000 rpm). Collect the supernatant carefully. One part of the package is to be tested, and the rest is frozen for use. 6. The specimens should be extracted as soon as possible after collection, and the extraction should be carried out according to the 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 °C, but repeated freezing and thawing should be avoided. 7. Samples containing NaN3 cannot be detected because NaN3 inhibits horseradish peroxidase (HRP) activity. Steps: Precautions: 10. In the case of an English manual, the English manual shall prevail. Calculation : Taking the concentration of the standard as the abscissa and the OD as the ordinate, draw a standard curve on the coordinate paper, and find the corresponding concentration from the standard curve according to the OD value of the sample; multiply by the dilution factor; or use the concentration of the standard Calculate the linear regression equation of the standard curve with the OD value, substitute the OD value of the sample into the equation, calculate the sample concentration, and multiply by the dilution factor, which is the actual concentration of the sample. Kit performance: 1. The linear regression coefficient of the sample and the expected concentration correlation coefficient R value is 0.990 or more. 2. Within and between batches should be less than 9% and 11% respectively examination range: 10 IU/L -300 IU/L Storage conditions and expiration date: 1. Kit storage: 2-8 ° C. 2. 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