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Cloning and expression of gp37 gene of avian leukosis virus subgroup J / 病毒学报
Chinese Journal of Virology ; (6): 178-184, 2012.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-354751
Responsible library: WPRO
ABSTRACT
The transmembrane protein (TM) encoded by gp37 gene plays a critical role when virus fusion with cell membrane occurs. Several highly conserved regions in TM are important targets for antivirus studies. Studies on structure and function of TM will provide basic information for anti-retrovirus, especially for avian leukosis virus. In the study, gp37 gene was amplified by PCR from the Chinese strain ALV-J-WS0701. The gp37 gene was cloned into pMD18-T vector, and was sequenced. Then, pFast-BacHTb-gp37 vector was constructed and expressed by baculovirus expression vector system. The expression product of gp37 gene was analyzed by indirect immunofluorescence assay and Western blot. The results showed that positive green fluorescence was present in sf9 cells infected with recombinant virus and a protein band with a molecular weight of 21kD was present in Western blot. It is concluded that gp37 gene was expressed in sf9 cells infected with recombinant virus successfully.
Subject(s)
Full text: Available Database: WPRIM (Western Pacific) Main subject: Virology / Avian Leukosis / Gene Expression / Cell Line / Chickens / Viral Envelope Proteins / Classification / Cloning, Molecular / Avian Leukosis Virus / Spodoptera Limits: Animals Language: Chinese Journal: Chinese Journal of Virology Year: 2012 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Virology / Avian Leukosis / Gene Expression / Cell Line / Chickens / Viral Envelope Proteins / Classification / Cloning, Molecular / Avian Leukosis Virus / Spodoptera Limits: Animals Language: Chinese Journal: Chinese Journal of Virology Year: 2012 Document type: Article
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