Cloning and Sequence Analysis of Hog Cholera Virus(HCV) E2 Gene

돼지 콜레라 바이러스 E2 유전자의 클로닝 및 염기서열분석

  • 이영기 (한국인삼연초연구원 원료연구부) ;
  • 강신웅 (한국인삼연초연구원 원료연구부) ;
  • 김선원 (한국인삼연초연구원 원료연구부) ;
  • 박성원 (한국인삼연초연구원 원료연구부) ;
  • 이종철 (한국인삼연초연구원 원료연구부) ;
  • 이청호 (한국인삼연초연구원 원료연구부)
  • Published : 2001.12.01

Abstract

Hog cholera virus(HCV) was purified from virus infected Bovine kidney cells. From this virus, total protein was analyzed by SDS-PAGE gel electrophoresis and about 55 kDa band of E2 envelope protein was detected. The viral RNA was purified and E2 cDNA was amplified by RT-PCR. E2 cDNA fragment was cloned to PCRII-TOPO cloning vector and named pE2. The analysis of nucleotide sequence showed that this E2 cDNA fragment inserted into pE2 was 1191 nucleotides long and coded 397 amino acids.

Keywords

References

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