论文部分内容阅读
利用硫氰酸胍裂解病毒和二氧化硅颗粒能够特异性吸附核酸的特性,将二氧化硅悬液、裂解液及肝炎病毒感染血清共同保温,病毒裂解释放出的核酸结合在二氧化硅颗粒上,经过双蒸水洗脱,所得核酸直接作PCR扩增。以该法提取感染血清样本中的HBVDNA或HCVRNA作为模板,再进行PCR扩增检测,产物在琼脂糖凝胶电泳上所见条带清晰。用本法检测HBsAg(+)/HBeAg(+)Auti-HBc(+)血清32例,阳性率为96%;检测抗-HCV阳性血清110例,阳性率为82.7%。该方法成本低,实验周期短,结果稳定。
The use of guanidine thiocyanate lytic virus and silica particles can be specific adsorption of nucleic acid characteristics, the suspension of silica, lysate and hepatitis virus infection sera co-incubation, viral lysis of the release of nucleic acid bound to the silica particles , After double distilled water, the resulting nucleic acid directly for PCR amplification. The HBVDNA or HCV RNA in the infected serum samples was extracted by this method as a template and then amplified by PCR. The bands of the product were clear on agarose gel electrophoresis. 32 cases of HBsAg (+) / HBeAg (+) Auti-HBc (+) serum were detected by this method, the positive rate was 96%. The positive rate of anti-HCV positive serum in 110 cases was 82.7%. The method has the advantages of low cost, short experiment period and stable result.