1999Joural of BiologyRequires access

Amplification and cloning of Glutathione-S-Transferase gene of Schistosoma japinicum (Chinese Stain)

Zuo-jun Jiang

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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.

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What this paper is about

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.

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Available 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.

Key concepts: Cloning (programming), Molecular biology, Biology, Gene, Polymerase chain reaction, Coding region, Glutathione S-transferase, Vector (molecular biology)

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Amplification and cloning of Glutathione-S-Transferase gene of Schistosoma japinicum (Chinese Stain) — Research Paper | ScholarLens