2012Journal of the South China Agricultural UniversityRequires access

Construction and expression of protokaryon expression plasmid for H and F genes of canine distemper virus isolated from mink.

Su Fengyan, Wen Tiefeng, Zong Ying, Quankai Wang

Open publisher page 0 citations

Abstract

H and F genes were obtained by digesting the cloning plasmid pMD-18T-H and pMD-18T-F respectively.The recombinant protokaryon expression plasmids pET28a-H and pET28a-F were constructed by sub-cloning the objective gene into pET28a(+) vector.Recombinant protokaryon expression plasmids pET28a-H and pET28a-F were transformed into Escherichia coli Rosetta2(DE3) cell.Target genes were successfully expressed by SDS-PAGE detection.The size of the recombinant fusion proteins was 31 400(H) and 38 200(F) respectively.The recombinant fusion proteins showed positive reaction to anti-CDV canine serum by Western-blot detection.

About this research paper

What this paper is about

H and F genes were obtained by digesting the cloning plasmid pMD-18T-H and pMD-18T-F respectively.The recombinant protokaryon expression plasmids pET28a-H and pET28a-F were constructed by sub-cloning the objective gene into pET28a(+) vector.Recombinant protokaryon expression plasmids pET28a-H and pET28a-F were transformed into Escherichia coli Rosetta2(DE3) cell.Target genes were successfully expressed by SDS-PAGE detection.The size of the recombinant fusion proteins was 31 400(H) and 38 200(F) respectively.The recombinant fusion proteins showed positive reaction to anti-CDV canine serum by Western-blot detection.

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

H and F genes were obtained by digesting the cloning plasmid pMD-18T-H and pMD-18T-F respectively.The recombinant protokaryon expression plasmids pET28a-H and pET28a-F were constructed by sub-cloning the objective gene into pET28a(+) vector.Recombinant protokaryon expression plasmids pET28a-H and pET28a-F were transformed into Escherichia coli Rosetta2(DE3) cell.Target genes were successfully expressed by SDS-PAGE detection.The size of the recombinant fusion proteins was 31 400(H) and 38 200(F) respectively.The recombinant fusion proteins showed positive reaction to anti-CDV canine serum by Western-blot detection.

Key concepts: Recombinant DNA, Plasmid, Molecular biology, Cloning (programming), Mink, Biology, Canine distemper, Gene

Related papers

Back to paper searchBrowse research topicsOriginal source
Construction and expression of protokaryon expression plasmid for H and F genes of canine distemper virus isolated from mink. — Research Paper | ScholarLens