2006Chinese Journal of Clinical Laboratory ScienceRequires access

Rapid detection of GSTM1 polymorphisms using SYBR green I and melting curve analysis

Xiao Wang

Open publisher page 0 citations

Abstract

Objective To establish a method to detect the glutathione stransferase(GST) M1 gene polymorphisms rapidly and to apply preliminary for detection.Methods GSTM1 gene and internal control gene CYP1A1 were amplified by multi-PCR with appropriate fluorescent dye SYBR green I in the reaction system,The changes of fluorescence values were recorded from 65 ℃ to 95 ℃ by a rate of(0.1 ℃/s) when PCR was just completed.Results There were two peaks in the melting curve of GSTM1~+ genotype,but only a single peak occurred for the GSTM1-genotype.The temperatures of two peaks corresponded to the expected Tm.agarose gel electrophoresis analysis demonstrated that these peaks correspond to the bands of the predicted molecular size.The detection can be completed within an hour after DNA was extracted.Conclusion Melting curve analysis combined with SYBR green I is a easy,rapid,accurate methodfor detection of GSTM1 gene polymorphisms.

About this research paper

What this paper is about

Objective To establish a method to detect the glutathione stransferase(GST) M1 gene polymorphisms rapidly and to apply preliminary for detection.Methods GSTM1 gene and internal control gene CYP1A1 were amplified by multi-PCR with appropriate fluorescent dye SYBR green I in the reaction system,The changes of fluorescence values were recorded from 65 ℃ to 95 ℃ by a rate of(0.1 ℃/s) when PCR was just completed.Results There were two peaks in the melting curve of GSTM1~+ genotype,but only a single peak occurred for the GSTM1-genotype.The temperatures of two peaks corresponded to the expected Tm.agarose gel electrophoresis analysis demonstrated that these peaks correspond to the bands of the predicted molecular size.The detection can be completed within an hour after DNA was extracted.Conclusion Melting curve analysis combined with SYBR green I is a easy,rapid,accurate methodfor detection of GSTM1 gene polymorphisms.

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

Objective To establish a method to detect the glutathione stransferase(GST) M1 gene polymorphisms rapidly and to apply preliminary for detection.Methods GSTM1 gene and internal control gene CYP1A1 were amplified by multi-PCR with appropriate fluorescent dye SYBR green I in the reaction system,The changes of fluorescence values were recorded from 65 ℃ to 95 ℃ by a rate of(0.1 ℃/s) when PCR was just completed.Results There were two peaks in the melting curve of GSTM1~+ genotype,but only a single peak occurred for the GSTM1-genotype.The temperatures of two peaks corresponded to the expected Tm.agarose gel electrophoresis analysis demonstrated that these peaks correspond to the bands of the predicted molecular size.The detection can be completed within an hour after DNA was extracted.Conclusion Melting curve analysis combined with SYBR green I is a easy,rapid,accurate methodfor detection of GSTM1 gene polymorphisms.

Key concepts: Melting curve analysis, SYBR Green I, Agarose gel electrophoresis, Molecular biology, Genotype, Fluorescence, Agarose, Biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Rapid detection of GSTM1 polymorphisms using SYBR green I and melting curve analysis — Research Paper | ScholarLens