2001Unpublished venueRequires access

Cloning and expressing of HIV-1gp41N and C pep-tide gene

Qian Zhao

Open publisher page 0 citations

Abstract

Aim To express N and C peptide genes of HIV-1gp41in E.Coli JM109.Methods N and C peptide genes of HIV -1gp41were amplified from plasmid containing c DNA of HIV -1gp160gene by PCR and cloned into prokaryotic expression vector pGEx-4T -1.The cloned genes were subcloned into pGEM7zf(+)and sequenced.Expression of the cloned genes were induced in E.coli JM109and analysed on SDS -PAGE.Results The N and C peptide genes were amplified and cloned successfully,and which was confirm ed by restriction endonuclease and sequence analysis.The fused GST -N a nd GST -C were expressed successfully identified by SDS -PAGE.Conclusion The expression of N and C peptide genes of HIV -1gp41have laid the foundation for further investigation.

About this research paper

What this paper is about

Aim To express N and C peptide genes of HIV-1gp41in E.Coli JM109.Methods N and C peptide genes of HIV -1gp41were amplified from plasmid containing c DNA of HIV -1gp160gene by PCR and cloned into prokaryotic expression vector pGEx-4T -1.The cloned genes were subcloned into pGEM7zf(+)and sequenced.Expression of the cloned genes were induced in E.coli JM109and analysed on SDS -PAGE.Results The N and C peptide genes were amplified and cloned successfully,and which was confirm ed by restriction endonuclease and sequence analysis.The fused GST -N a nd GST -C were expressed successfully identified by SDS -PAGE.Conclusion The expression of N and C peptide genes of HIV -1gp41have laid the foundation for further investigation.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Aim To express N and C peptide genes of HIV-1gp41in E.Coli JM109.Methods N and C peptide genes of HIV -1gp41were amplified from plasmid containing c DNA of HIV -1gp160gene by PCR and cloned into prokaryotic expression vector pGEx-4T -1.The cloned genes were subcloned into pGEM7zf(+)and sequenced.Expression of the cloned genes were induced in E.coli JM109and analysed on SDS -PAGE.Results The N and C peptide genes were amplified and cloned successfully,and which was confirm ed by restriction endonuclease and sequence analysis.The fused GST -N a nd GST -C were expressed successfully identified by SDS -PAGE.Conclusion The expression of N and C peptide genes of HIV -1gp41have laid the foundation for further investigation.

Key concepts: Cloning (programming), Restriction enzyme, Gene, Molecular biology, Biology, Plasmid, Multiple cloning site, Molecular cloning

Related papers

Back to paper searchBrowse research topicsOriginal source
Cloning and expressing of HIV-1gp41N and C pep-tide gene — Research Paper | ScholarLens