大鼠熱休克蛋白27(HSP-27)檢測
參考價 | ¥ 1800 |
訂貨量 | ≥1 |
- 公司名稱 北京方程嘉鴻科技有限公司
- 品牌
- 型號
- 產(chǎn)地 北京
- 廠商性質 經(jīng)銷商
- 更新時間 2018/1/10 17:25:44
- 訪問次數(shù) 381
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規(guī)格 | 96T | 貨號 | ELISA |
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大鼠熱休克蛋白27(HSP-27)檢測
北京方程生物公司銷售Hu人環(huán)磷酰胺(CTX)試劑盒,英文名稱:Human Cyclin-D2 ELISA Kit
![大鼠熱休克蛋白27(HSP-27)檢測](https://img48.chem17.com/df293c85a2d9f0fb2ee587200980c9c37b82859b7829dc438813d2a050de1243e9f6ec89c13fd5f0.jpg)
After incubation, transfer the reaction mixtures to the second antigen-coated microtitre plate. The ELISA assay using this second plate will now be performed exactly as for the first microtitre plate. The purpose of the second ELISA assay is to check that only a small fraction of the free antibody is captured on the first microtitre plate and, therefore, no readjustment of the equilibrium occurred during the first capture step. Wash extensively the first ELISA plate and perform the remaining steps of an ELISA procedure, aimed at the determination of the antibody binding to the coated antigen. Develop the ELISA with a suitable chromogenic, fluorogenic or chemiluminescent substrate, and measure the individual wells with an appropriate ELISA plate reader. The highest ELISA signal should be observed at low concentrations of antigen. No ELISA signal should be observed at high concentrations of antigen. The concentration of antigen at which the half-maximal ELISA signal is detected corresponds to the dissociation constant Kd. Alternatively, the Kd value can be obtained by fitting the ELISA signal of the individual wells to the equation: Kd = [A][B]/[AB] .;Competitive ELISA1. Coat Nunc immuno-module plates overnight, in usual manner. 2. Set up competition assay between antibody and competing substance :- Prepare a 1:2 serial dilution of the competitive substance from 480 to 0.4 ng/ml. Add 50ul of each of the above dilutions to 25ul of 3x strength titre of antibody (i.e. a solution 3 x the titre giving 50% inhibition on direct ELISA), in sealed tubes. 3. Incubate overnight at room temperature. 4. Set up competition between unknown concentration of competitive substance and antibody as above.
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Cover the plate with Parafilm and incubate for 2 hours at 37°C, followed by an overnight incubation at 4°C. Cover the plate tightly to avoid evaporation. Store at 4°C. The plate(s) will remain usable for about one month.
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