First, the application of the original ELISA kit
Using the genetic site-directed modification technology CRISPR-Cas system, precise localization of gene modifications or knockouts on haploid stem cells can be performed quickly and efficiently, and the treated cells can maintain haploid and pluripotent states. More importantly, this work demonstrates that rat haploid embryonic stem cells also have the ability to "fertilize" sperm and oocytes and produce healthy rats.
Second, how to judge the original ELISA kit test results
1. Measured method: After the substrate was added and the reaction was terminated, the color of the positive hole was visually observed to be deeper than that of the negative control; if it was close to the color of the negative control, it was judged to be negative.
2. The OD value of the sample well is greater than the negative control OD value +2 to 3 SD as the threshold for the positive result.
3. P/N value (positive hole OD value / negative hole OD value) is greater than or equal to 2.1 is positive; P/N value is less than 2.1, but greater than 1.5 is suspicious; P/N is less than 1.5 is negative.
4. Quantitative measurement results The content of the analyte in the sample is calculated from the standard curve.
Third, research on the original ELISA kit shows
The imported rat elisa kit was studied and the level of rat sex hormone binding globulin (SHBG) elisa kit in the specimen was determined by double antibody sandwich method. The purified rat rat sex hormone binding globulin (SHBG) elisa kit is coated with a microplate to prepare a solid phase antibody, and the sex hormone binding globulin (SHBG) elisa reagent is sequentially added to the microwell of the coated monoclonal antibody. The cassette is then combined with an HRP-labeled sex hormone-binding globulin (SHBG) elisa kit antibody to form an antibody-antigen-enzyme-labeled antibody complex, which is thoroughly washed and then added to the substrate TMB 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 the sex hormone binding globulin (SHBG) elisa kit in the sample. The absorbance (OD value) was measured with a microplate reader at a wavelength of 450 nm, and the concentration of the rat sex hormone binding globulin (SHBG) elisa kit in the sample was calculated from a standard curve.
Shanghai Jinma Research Center recommends that customers choose the original Elisa kit from the following points:
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