一、概况:为了使实验室准确报告HBsAg的实验结果,不使造成人为的差错,我在实际操作中发现,操作时混入红血球、严重溶血标本,对结果有影响,应舍去,重新抽样。供其它基层实验室参考。因说明书上未注明注意事项。二、试剂来源:亚利生物工程有限公司提供,《快速EIA薄膜法检测HBsAg诊断试剂盒》。生产日期1992年8月7号,批号为920807,有效期半年。三、实验:于92年8月29号用微量采血对宾馆 First, an overview: In order to accurately report the laboratory results of HBsAg experiments, without causing human error, I found in practice, the operation mixed with red blood cells, severe hemolysis specimens, the results have an impact, should be discarded and resampled. For other grassroots laboratory reference. Because the instructions did not indicate the precautions. Second, the source of reagents: Biological Engineering Co., Ltd. Yali, “Rapid EIA membrane detection HBsAg diagnostic kit.” Production date August 7, 1992, batch number 920,807, valid for six months. Third, the experiment: on August 29, 92 with a trace of blood on the hotel