Foundation of Polypeptide: N-acetylgalactosaminyltransferases cDNA Library by TOPO-TA Cloning
Wu Shi
Abstract
Wu Shi
Abstract
Objective: To make the cDNA library by TOPO-TA cloning in order to analyze the differences of N-acetylgalactosaminyltransferases gene expression profile in different human tumor cells. Methods: Mainly by means of PCR and TOPO-TA cloning. Results: Through patterns of electrophoresis, it was rudimentarily proved that N-acetylgalactosaminyltransferases gene family cDNA had been successfully amplified and the cDNA library had also been made. Conclusion: N-acetylgalactosaminyltransferases gene family cDNA has been amplified successfully and the cDNA library has been made by means of TOPO-TA cloning.
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.
Objective: To make the cDNA library by TOPO-TA cloning in order to analyze the differences of N-acetylgalactosaminyltransferases gene expression profile in different human tumor cells. Methods: Mainly by means of PCR and TOPO-TA cloning. Results: Through patterns of electrophoresis, it was rudimentarily proved that N-acetylgalactosaminyltransferases gene family cDNA had been successfully amplified and the cDNA library had also been made. Conclusion: N-acetylgalactosaminyltransferases gene family cDNA has been amplified successfully and the cDNA library has been made by means of TOPO-TA cloning.
Key concepts: Complementary DNA, cDNA library, Cloning (programming), Library, Molecular biology, Molecular cloning, Gene, Biology