Amplification and cloning of Glutathione-S-Transferase gene of Schistosoma japinicum (Chinese Stain)
Zuo-jun Jiang
Abstract
Zuo-jun Jiang
Abstract
SjcDNA first strand synthesis was driven by superscript Ⅱ RT using adult worm RNA as template.Specific primers was designed and synthesized.Coding region gene of SjGST was amplified by PCR.The product from PCR was cloned into pGEM-T-GST vector.The cloning vector pGEM-T-GST was identified by restriction analysis and PCR.The results demonstrated that pGEM-T-GST was successfully constructed and provided the basis for further study on GST expression and its immunological diagnosis and prevention.
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.
SjcDNA first strand synthesis was driven by superscript Ⅱ RT using adult worm RNA as template.Specific primers was designed and synthesized.Coding region gene of SjGST was amplified by PCR.The product from PCR was cloned into pGEM-T-GST vector.The cloning vector pGEM-T-GST was identified by restriction analysis and PCR.The results demonstrated that pGEM-T-GST was successfully constructed and provided the basis for further study on GST expression and its immunological diagnosis and prevention.
Key concepts: Cloning (programming), Molecular biology, Biology, Gene, Polymerase chain reaction, Coding region, Glutathione S-transferase, Vector (molecular biology)