2005Xibei Nong-Lin Keji Daxue xuebao. Ziran kexue banRequires access

Rapid confirmation of the transgenic wheat lines by polymerase chain reaction(PCR)

Meng Chaomin, Xiaodong Zhang, Tianyou Chen

Open publisher page 0 citations

Abstract

A new rapid DNA extraction method was developed for transgenic wheats identified by PCR.The result showed that this method was convenient,quick and effective.The quality of DNA extracted using this method was suitable for PCR analysis.An optimal reaction sytstem suitable for alien lysine-rich gene PCR was also established in this research:10×Reaction Buffer 2.5 μL,MgCl_2 25 mmol/L,dNTPs(2.5) mmol/L,Genmonic DNA 30-60 ng,primers 1.2 μmol/L,Taq enzyme 1 U,ddH_2O to 25 μL.

About this research paper

What this paper is about

A new rapid DNA extraction method was developed for transgenic wheats identified by PCR.The result showed that this method was convenient,quick and effective.The quality of DNA extracted using this method was suitable for PCR analysis.An optimal reaction sytstem suitable for alien lysine-rich gene PCR was also established in this research:10×Reaction Buffer 2.5 μL,MgCl_2 25 mmol/L,dNTPs(2.5) mmol/L,Genmonic DNA 30-60 ng,primers 1.2 μmol/L,Taq enzyme 1 U,ddH_2O to 25 μL.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

A new rapid DNA extraction method was developed for transgenic wheats identified by PCR.The result showed that this method was convenient,quick and effective.The quality of DNA extracted using this method was suitable for PCR analysis.An optimal reaction sytstem suitable for alien lysine-rich gene PCR was also established in this research:10×Reaction Buffer 2.5 μL,MgCl_2 25 mmol/L,dNTPs(2.5) mmol/L,Genmonic DNA 30-60 ng,primers 1.2 μmol/L,Taq enzyme 1 U,ddH_2O to 25 μL.

Key concepts: Polymerase chain reaction, DNA, Molecular biology, DNA extraction, Chromatography, Polymerase chain reaction optimization, Extraction (chemistry), Chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Rapid confirmation of the transgenic wheat lines by polymerase chain reaction(PCR) — Research Paper | ScholarLens