Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi
October 2008
Objective: To explore the relation between hepatitis B virus DNA load and genotype with the level of large envelope protein.
Methods: Serum HBV DNA was quantitively detected by using real time polymerase chain reaction (RT-PCR). The LHBs were detected by using enzyme linked immuno sorbent assay (ELISA) and HBV markers were detected by time differentiate immunofluorescence assay in 140 serum samples collected from chronic hepatitis B patients.
Zhonghua Gan Zang Bing Za Zhi
July 2003