方案摘要
方案下载应用领域 | 生物产业 |
检测样本 | |
检测项目 | |
参考标准 | 文献 |
Important notes 1.The kit takes out from the refrigeration environment should be balanced15-30 minutes in the room temperature, ELISA plates coated if has not useup after opened, the plate should be stored in Sealed bag. 2.washing buffer will Crystallization separation, it can be heated the waterhelps dissolve when dilute . Washing does not affect the result. 3.add Sample with sampler Each step, And proofread its accuracy frequently,avoids the experimental error. add sample within 5 mins, if the number ofsample is much , recommend to use Volley . 4.if the testing material content is excessively higher (The sample OD isbigger than the first standard well ),please dilute Sample (n-fold), Pleasediluente and multiplied by the dilution factor.(×n×5). 5.Closure plate membrane only limits the disposable use, to avoidcLTs-contamination. 6.The substrate evade the light preservation. 7.Please according to use instruction strictly, The test result determinationmust take the microtiter plate reader as a standard. 8.All samples, washing buffer and each kind of reject should according toinfective material process. 9.Do not mix reagents with those from other lots.
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