Method 1 Double antibody sandwich method 1. Coating: Dilute the antibody to protein content of 1-10 μg / ml with 0.05MPH9. Carbonate coating buffer. Add 0.1ml to the reaction well of each polystyrene plate, overnight at 4 ℃. The next day, the solution in the well was discarded and washed 3 times with washing buffer for 3 minutes each time. (Referred to as washing, the same below). 2. Add sample: add 0.1ml of the diluted test sample to the above-mentioned coated wells and incubate at 37 ℃ for 1 hour. Then wash. (Make blank wells, negative control wells and positive control wells at the same time). 3. Add enzyme-labeled antibody: add 0.1ml of freshly diluted enzyme-labeled antibody (dilution after titration) to each reaction well. Incubate at 37 ° C for 0.5 to 1 hour and wash. 4. Add substrate to develop color: add 0.1ml of temporarily prepared TMB substrate solution to each reaction well at 37 ℃ for 10 to 30 minutes. 5. Terminate the reaction: Add 0.05ml of 2M sulfuric acid to each reaction well. 6. Judgment of results: The results can be directly observed with the naked eye on a white background: the darker the color of the reaction well, the stronger the positive degree, and the negative reaction is colorless or extremely light. According to the depth of the color, "+", "-" Indicates. OD value can also be measured: on the ELISA detector, at 450nm (410nm if ABTS color is developed), the OD value of each well is measured after zero adjustment with a blank control well, if it is greater than 2.1 times the specified negative control , That is positive. Method two: Indirect method 1. Dilute the known antigen to 1 ~ 10μg / ml with coating buffer, add 0.1ml to each well, overnight at 4 ℃; 2. Wash 3 times the next day; 3. Add a certain dilution of the sample to be tested (Unknown antibody) 0.1ml in the above-coated reaction wells, incubate at 37 ° C for 1 hour, wash; 4. (Also do blank, negative and positive well control) in the reaction wells, add freshly diluted enzyme label 0.1ml of secondary antibody (anti-antibody); incubate at 5.37 ° C for 30-60 minutes and wash; 6. 'Last wash with DDW. Interleukin 6Elisa kit related products: human interleukin 12 (IL-12 / P70) ELISA kit human interleukin 12 (IL-12 / P40) ELISA kit human interleukin 11 (IL-11) ELISA kit human interleukin 10 (IL- 10) ELISA kit chicken interleukin 6 (IL-6) ELISA kit chicken interleukin 4 (IL-4) ELISA kit chicken interleukin 2 (IL-2) ELISA kit rat interleukin 6 (IL-6) ELISA kit Rat Interleukin 4 (IL-4) ELISA Kit Rat Interleukin 2 (IL-2) ELISA Kit Rat Interleukin 1α (IL-1α) ELISA Kit Rat Interleukin 18 (IL-18) ELISA Kit Rat Interleukin 10 (IL-10) ELISA Kit Mouse Interleukin 6 (IL-6) ELISA Kit Mouse Interleukin-5 (IL-5) ELISA Kit Mouse Interleukin 4 (IL-4) ELISA Kit Mouse Interleukin 3 (IL-3) ELISA kit mouse interleukin 2 (IL-2) ELISA kit mouse interleukin 1α (IL-1α) ELISA kit order method: 1. After confirming the product, you can directly contact us online, or Contact by phone to confirm the product you purchased.
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