This is an important provision in Circular 13/2013/TT-BTNMT of the Ministry of Natural Resources and Environment of Vietnam stipulating the technical process and economic-technical norms in detecting genetically modified organisms through qualitative and quantitative analysis of Deoxyribonucleic Acid, issued on March 31, 2014.
DNA quality and quantity determination in Vietnam
To be specific:, in the Technical Process and Economic-Technical Norms for detecting genetically modified organisms by qualitative and quantitative analysis methods of Deoxyribonucleic Acid issued with Circular 13/2013/TT-BTNMT, it is stipulated that the quality, quantity, and integrity of DNA samples greatly affect the results of the analysis method. According to TCVN 7606:2007 (ISO 21571), the main steps in the process of DNA quality and quantity determination include:
- Preparation of tools and chemicals;
- Electrophoresis of DNA on agarose gel
;- Determination of DNA quantity using a spectrophotometer;
- Result analysis and processing.
There are 2 common methods to determine the concentration of DNA in the solution: Electrophoresis method and spectrophotometric DNA quantity determination method.
Additionally, the PCR method is commonly used to replicate a gene segment using a primer pair specifically designed for this gene sequence. In this case, PCR is used to detect and identify genetically modified organisms, also known as qualitative PCR. According to TCVN 7605:2007 (ISO 21569), the main steps to detect and identify genetically modified organisms using PCR technique include:
- Preparation of tools and chemicals;
- Designing primer pairs to amplify the gene segment;
- Performing PCR reaction;
- Analyzing and processing results with electrophoresis on agarose gel.
For more details, refer to Circular 13/2013/TT-BTNMT, effective from August 5, 2013.
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