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SN/T 2584-2010 English PDF

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SN/T 2584-2010: Protocol of real time polymerase chain reaction for detecting genetically modified components in rice and its derived products
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Basic data

Standard ID SN/T 2584-2010 (SN/T2584-2010)
Description (Translated English) Protocol of real time polymerase chain reaction for detecting genetically modified components in rice and its derived products
Sector / Industry Commodity Inspection Standard (Recommended)
Classification of Chinese Standard X11
Classification of International Standard 67.060
Word Count Estimation 10,120
Date of Issue 2010-05-27
Date of Implementation 2010-12-01
Quoted Standard GB 6682; SN/T 1193; SN/T 1194
Regulation (derived from) National Quality Inspection (2010) 290; industry standard filing Notice 2010 No. 10 (No. 130 overall)
Issuing agency(ies) General Administration of Customs
Summary This standard specifies the rice and rice products in GMO detection methods. This standard applies to transgenic Bt rice (TT51-1, Kemingdao, �� excellent Kefeng the 6th) and herbicide resistant transgenic rice (LLRICE62, LLRICE601) detection, but also for GMO detection in rice products.

SN/T 2584-2010: Protocol of real time polymerase chain reaction for detecting genetically modified components in rice and its derived products


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Protocol of real time polymerase chain reaction for detecting genetically modified components in rice and its derived products People's Republic of China Entry-Exit Inspection and Quarantine Standards Genetically Modified Rice and Its Products Real-time PCR detection method Issued on. 2010-05-27 2010-12-01 implementation People's Republic of China The State Administration of Quality Supervision, Inspection and Quarantine released

Foreword

This standard was drafted in accordance with GB/T 1.1-2009 given rules. This standard is proposed and managed by the National Certification and Accreditation Administration Committee. This standard was drafted. Xiamen, People's Republic of China Exit Inspection and Quarantine, Chinese Academy of Inspection and Quarantine, the People's Republic of China And Beijing, China Entry-Exit Inspection and Quarantine Hubei People's Republic of China. The main drafters of this standard. Chen Yun, Liang Miao, Chen Shuangya, Wang Zhenhua, Li Ling, Huang Wensheng, Hu small bell, water Zhu Fang, Chen Hongjun. Genetically Modified Rice and Its Products Real-time PCR detection method

1 Scope

This standard specifies the method for the detection of rice and rice products genetically modified ingredients. This standard applies to transgenic Bt rice (TT51-1, Kemingdao, Ⅱ excellent Kefeng 6) and herbicide-tolerant transgenic rice (LLRICE62, LLRICE601) detection, but also for the detection of genetically modified rice products.

2 Normative references

The following documents for the application of this document is essential. For dated references, only the dated version suitable for use herein Member, undated references, the latest edition (including any amendments) applies to this document. GB 6682 analytical laboratory use specifications and test methods SN/T 1193 genetic testing laboratory technical requirements Detection sampling and sample preparation method SN/T 1194 in genetically modified plants and their products

3 Abbreviations

The following abbreviations apply to this document. 3.1 crylAc gene crylAcgene Encoding Bacillus thuringiensis (Bacillusthuringiensis) gene CrylAc insecticidal crystal protein. 3.2 crylAb gene crylAbgene Encoding Bacillus thuringiensis (Bacillusthuringiensis) gene CrylAb insecticidal crystal protein. 3.3 crylAb/crylAc fusion gene crylAb/crylAcfusiongene crylAb artificial gene and gene splicing crylAc formation genes. 3.4 sps gene sucrosephosphatesynthase Sucrose phosphate synthase gene, the rice used in this standard within the standard gene. 3.5 gos9 gene gosgene The roots of a rice gene expression in this standard is used as internal standard gene in rice. 3.6 PLD gene phospholipaseDgene Phospholipase D gene. 3.7 Ct values cyclethreshold When the number of cycles for each reaction tube fluorescent signal reaches the set threshold experienced by some brands of quantitative PCR instrument, also known as Cp (Crosspoint) value.


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