摘要
本文首次采用SP_(65)特殊质粒与人类的乙型肝类病毒DNA(HBVDNA)重组,制备了Bio-HBVRNA探针,能特异地与HBVDNA杂交。将该探针与缺口转移(NicHranalatiOn)方法标记的m小HBVDNA探针进行了比较。结果显示出Bio-HBVRNA探针比Bio-HBVDNA探针的敏感性提高10倍。并分别应用两种探针同时检测70例己肝病人血清中HBVDNA,阳性率各为31.42%、28.57%(P>0.25).对Bio-HBVRNA探针应用于临床检测乙肝病毒DNA的效能也进行了初步探讨。
epotits B virus (HBV)RNA probes were synthesized in vitro by transcription from recombinantsbetween HBV DNA and the transcriptfon vector SP_(65).These probes can be labelled with biotin and behybridized spoifically with HBV DNA.Comparing with HBV DNA probe prepared by Nick-translation for detection of HBV DNA,HBVRNA probe are 10 times sensitive than that of HBV DNA.In addition,70 serum saniples of hepatitis B potients have been detected by hybridization withtwo probes.Pooitive proportion of HBV DNA corresponils to 31.42%, 28.57%(P>0.25).The clinical application of HBV RNA probes was discusseil preluninarily.
出处
《中国病毒学》
CSCD
1994年第2期95-99,共5页
Virologica Sinica
关键词
生物素探针
乙型肝炎病毒
RNA
HBV DNA,SP65 vector,Nick-translation,Biotin probe