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SN/T 4055-2014 English PDF

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SN/T 4055-2014: Detection method of norovirus in shellfish. Conventional RT-PCR and real-time RT-PCR
Status: Valid
Standard IDUSDBUY PDFLead-DaysStandard Title (Description)Status
SN/T 4055-2014289 Add to Cart 3 days Detection method of norovirus in shellfish. Conventional RT-PCR and real-time RT-PCR Valid

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Basic data

Standard ID: SN/T 4055-2014 (SN/T4055-2014)
Description (Translated English): Detection method of norovirus in shellfish. Conventional RT-PCR and real-time RT-PCR
Sector / Industry: Commodity Inspection Standard (Recommended)
Classification of Chinese Standard: X20
Classification of International Standard: 67.120.30
Word Count Estimation: 11,145
Date of Issue: 12/1/2014
Date of Implementation: 5/1/2015
Quoted Standard: GB/T 19495.2
Regulation (derived from): State-Quality-Inspection-accreditation [2014] 614
Issuing agency(ies): General Administration of Customs
Summary: This standard specifies the norovirus in shellfish common RT-PCR and real-time RT-PCR detection method. This standard applies to such as virus detection in shellfish promise.

SN/T 4055-2014: Detection method of norovirus in shellfish. Conventional RT-PCR and real-time RT-PCR


---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Detection method of norovirus in shellfish.Conventional RT-PCR and real-time RT-PCR People's Republic of China Entry-Exit Inspection and Quarantine Industry Standard Replace SN/T 1635-2005 Norovirus detection method in shellfish Ordinary RT-PCR method and real Time-fluorescent RT-PCR method Conventional RT-PCR and real-time RT-PCR Released on.2014-11-19 2015-05-01 implementation People's Republic The General Administration of Quality Supervision, Inspection and Quarantine issued

Foreword

This standard was drafted in accordance with the rules given in GB/T 1.1-2009. This standard replaces SN/T 1635-2005 "Norwalk virus detection method in shellfish, ordinary RT-PCR method and real-time fluorescence RT- PCR method. Compared with SN/T 1635-2005, the main technical changes of this standard are as follows. --- Modified the standard Chinese name; --- Modified the virus name, which was modified from Norovirus to Norovirus. This standard is proposed and managed by the National Certification and Accreditation Administration. This standard was drafted. Guangxi Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China, Shanghai Entry and Exit Inspection of the People's Republic of China Epidemic situation. The main drafters of this standard. Liu Junyi, Pan Liangwen, Li Xiang, Lu Rong, Wei Meiliang, Chen Lijun, Luo Zhaofei. The previous versions of the standards replaced by this standard are. ---SN/T 1635-2005. Norovirus detection method in shellfish Ordinary RT-PCR method and real Time-fluorescent RT-PCR method

1 Scope

This standard specifies the common RT-PCR and real-time fluorescent RT-PCR detection methods for Nobel virus in shellfish. This standard applies to the detection of Norovirus in shellfish.

2 Normative references

The following documents are indispensable for the application of this document. For dated references, only dated versions apply to this article. Pieces. For undated references, the latest edition (including all amendments) applies to this document. GB/T 19495.2 Technical requirements for testing laboratory of genetically modified products

3 Terms and definitions

The following terms and definitions apply to this document. 3.1 Real-time fluorescence RT-PCR real-timefluorescence RT-PCR The real-time fluorescent RT-PCR method is based on conventional RT-PCR and a specific fluorescent probe is added. The probe is a The oligonucleotide is labeled with a reporter group and a quenching fluorophore at each end. When the probe is intact, the fluorescent signal emitted by the reporter group is Quenching group absorption; during PCR amplification, the 5'-3' exonuclease activity of the Taq enzyme degrades the probe, allowing the reporter group and the quenching fluorophore Separation, so that the fluorescence monitoring system can receive the fluorescent signal, that is, every time a DNA strand is amplified, a fluorescent molecule is formed, and the fluorescence is realized. The accumulation of light signals is fully synchronized with the formation of the PCR product. 3.2 Ct value cyclethreshold The number of cycles experienced by the fluorescent signal in each reaction tube reaching the set domain value.

4 reagents

All experimental reagents were of analytical grade; unless otherwise stated, the experimental water was distilled or deionized water. 4.1 Norovirus positive specimens. provided by the designated unit of the General Administration of Quality Supervision, Inspection and Quarantine. -80 ° C low temperature refrigerator storage. 4.2 Glycine buffer. see A.1.1. 4.3 PEG8000 solution. see A.1.2. 4.4 50 x TAE buffer. see A.1.3. 4.5 Ethidium bromide solution (10 μg/μL). see A.1.4. 4.6 1.5% agarose gel containing 0.5 μg/mL ethidium bromide. see A.1.5. 4.7 10× loading buffer. see A.1.6.
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