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
Abstract
Su Fengyan, Wen Tiefeng, Zong Ying, Quankai Wang
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.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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