Objective To explore the effect of residual UDG on all dU-DNA PCR products. Methods The hybridization percentage of dU-DNA PCR products, which were stored at 37℃ for 20 hours as well as at -20℃,4℃,room temperature and 37℃,respectively, were detected by employing microplate hybridization technique. The effect of inactivating the products at 94 ℃ for 10 minutes on the activity of Taq polymerase was also analysed. Results Compared with the control, A value decreased by 13.281% and 20.557%, respectively after adding 0.2u and 10u UDG (P

Objective To develop a rapid specific method to detect HBV gene mutation by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Methords The patients of YMDD and YIDD mutation were detected by DNA sequencing.Results the DNA sequencing demonstrated that not only YMDD and YIDD/YVDD mutation, but LLLL,LMLL,DLHD,DMHD,LLAQ and LMAQ mutation were also detected in different hepatitis B patients. The results of PCR-RFLP indicated that there were different restricted sites in the distinct mutation.Conclusion The results above indicated that all these mutants exist in the initiator codon of ATG(Met). The mutation of LMLL DMHD LMAQ was associated with Lamivordin treatment. Whether mutation of Met links with the second replicating of HBV needs to be further studied.

AIM:To research the protection of Cistanchis glycosides on ethanol-induced liver damage in mice.METHODS:40 mice were divided into 4 groups in random,and administered by gavage for 4 weeks.Cistanchis glycosides were twice a day,ethanol were once a day.When time limit arrived,mice were weighted,the serum was afforded to detect the liver function index,liver homogenate were prepared for biochemical detections,liver remained were fixed for pathological investigation.RESULTS:When mice were damaged by ethanol,liver index,liver function index,contents of TG,TC,MDA and LPO were increased distinctly(P