SN/T 5334.3-2020Digital PCR detection method for genetically modified plant products - Part 3: Genetically modified corn (English PDF)
转基因植物产品的数字PCR检测方法 第3部分:转基因玉米
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Issued by
General Administration of Customs
Level / Type
National · Recommended
Issue date
December 30, 2020
Implementation date
July 1, 2021
Scope
SN/T 5334.3-2020 is the English-translated version of 转基因植物产品的数字PCR检测方法 第3部分:转基因玉米.
SN/T 5334.3-2020 — This document specifies the digital PCR quantitative detection method for genetically modified strains in maize. This document is applicable to the quantitative detection of 10 genetically modified strains in corn seeds and leaves. See Appendix A for the detection limits of this document.
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Document preview — SN/T 5334.3-2020
National Standard of the People's Republic of China
- ICS
- 65.020.01
- Classification
- B 16
Issued by: General Administration of Customs
Contents
- Foreword
- 1 Scope
- 2 Normative references
- 3 Terms and definitions
- 4 Principles of the method
- 5 Main equipment and reagents
- 6 Method operation steps
- 6.1 General operation steps
- 6.2 Digital PCR reaction system
- 6.3 Digital PCR reaction program
- 7 Judgment and expression of results
- 8 Anti-pollution measures
- 9 Sample storage
Foreword
SN/T 5334-2020 "Digital PCR Detection Method for Genetically Modified Plant Products" is divided into 8 parts.
--Part 1: General requirements and definitions;
--Part 2: Genetically modified soybeans;
--Part 3: Genetically modified corn;
--Part 4: Genetically modified rape;
--Part 5: Genetically modified cotton;
--Part 6: Genetically modified potatoes;
--Part 7: Genetically modified alfalfa;
--Part 8: Genetically modified sugar beet.
This document is part 3 of SN/T 5334-2020.
This document was drafted in accordance with the rules given in GB/T 1.1-2020.
1 Scope
This document specifies the digital PCR quantitative detection method for genetically modified strains in maize.
This document is applicable to the quantitative detection of 10 genetically modified strains in corn seeds and leaves. See Appendix A for the detection limits of this document.
2 Normative references
The contents of the following documents constitute the indispensable clauses of this document through normative references in the text. Among them, dated quotations Only the version corresponding to that date is applicable to this document; for undated references, the latest version (including all amendments) is applicable Used in this document.
SN/T 5334.1 Digital PCR method for quantitative detection of genetically modified products Part 1: General requirements and definitions
3 Terms and definitions
The terms and definitions defined in SN/T 5334.1 apply to this document.
4 Principles of the method
See SN/T 5334.1.
5 Main equipment and reagents
5.1 Endogenous gene and exogenous gene. the endogenous gene is maize high mobility group proteins (HMG. high mobility group proteins);
The foreign genes are lines 98140, DAS40278-9, VCO-01981-5 and MON87427 insertion site 5'end cross-border sequence, and Strains BVLA430101, Bt799, IE034, 12-5, C0010.3.7 and C0030.3.5 insert the 3'-end cross-border sequence at the insertion site. Primers and See Appendix A for the probe sequence.
5.2 For other equipment and reagent requirements, please refer to SN/T 5334.1.
6 Method operation steps
6.1 General operation steps
For general operation steps, please refer to SN/T 5334.1.
6.2 Digital PCR reaction system
See Table 1 for the preparation of real-time fluorescent PCR reaction system.
Note. It is recommended to use the digital PCR platform on the market for experiments
6.3 Digital PCR reaction program
See SN/T 5334.1 for other requirements, and see Table 2 for the digital PCR reaction program.
a. According to the requirements of different digital PCR platforms, the hot start step in the reaction program can be modified, but the thermal cycle (amplification) must not be modified step.
b. According to the requirements of different digital PCR platforms, it is possible to perform post-processing after the thermal cycling (amplification) step, which can be performed according to the requirements of different platforms.
Seek to proceed.
7 Judgment and expression of results
See SN/T 5334.1 for calculation of results.
The results are expressed as follows.
- Both the internal standard gene and the foreign gene in the test result meet the negative and blank quality control requirements, indicating that no corn has been detected the endogenous gene Adh1, expressed as "no corn component detected";
- In the test results, the internal standard gene result is positive, but the foreign gene meets the quality control requirements of negative and blank, said Genetic strain";
- In the test results, both the internal standard gene and the exogenous genome meet the quality control requirements of the digital PCR test of the sample, indicating that
8 Anti-pollution measures
The anti-pollution measures are specified in SN/T 5334.1.
9 Sample storage
For sample storage, see SN/T 5334.1.
Appendix A
(Informative appendix) Primer probe sequence, reaction program and detection limit
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This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 5 pages — is available in the English PDF.
Referenced standards
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Related Standards
SN/T 5334.1-2020 — Digital PCR detection method for genetically modified plant products - Part 1: General requirements and definitions
SN/T 5334.2-2020 — Digital PCR Detection Method of Genetically Modified Plant Products - Part 2: Genetically Modified Soybean
SN/T 5334.4-2020 — Digital PCR Detection Method for Genetically Modified Plant Products - Part 4: Genetically Modified Rape
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