Clone and Prokaryotic Expression of Non-Structure Protein 3AB & 3A Genes in Foot-and-Mouth Disease
Xianfeng Zhang
Abstract
Xianfeng Zhang
Abstract
Based on the construction of template of non-structure protein 3ABC and plasmid pGEM-T-3ABC,the exceptional primers were designed and amplified by RT-PCR to get the non-structure protein 3AB and 3A genes.They were directed to be cloned into prokaryotic expression carrier pET-28a and pET-41a respectively.The recombinant plasmids were transformed into hose BL21,and the target proteins were induced by IPTG in BL21.The expressed proteins were examined by SDS-PAGE and Western blotting.The result showed that recombinant proteins were expressed in E.coli successfully.
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.
Based on the construction of template of non-structure protein 3ABC and plasmid pGEM-T-3ABC,the exceptional primers were designed and amplified by RT-PCR to get the non-structure protein 3AB and 3A genes.They were directed to be cloned into prokaryotic expression carrier pET-28a and pET-41a respectively.The recombinant plasmids were transformed into hose BL21,and the target proteins were induced by IPTG in BL21.The expressed proteins were examined by SDS-PAGE and Western blotting.The result showed that recombinant proteins were expressed in E.coli successfully.
Key concepts: Recombinant DNA, Plasmid, Gene, clone (Java method), lac operon, Biology, Molecular biology, Blot