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Loop-mediated isothermal amplification detection method at frontier port--Part 8: Chikungunya virus
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SN/T 3306.8-2017
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Basic data Standard ID | SN/T 3306.8-2017 (SN/T3306.8-2017) | Description (Translated English) | Loop-mediated isothermal amplification detection method at frontier port--Part 8: Chikungunya virus | Sector / Industry | Commodity Inspection Standard (Recommended) | Classification of Chinese Standard | C62 | Word Count Estimation | 10,166 | Date of Issue | 2017-05-12 | Date of Implementation | 2017-12-01 | Regulation (derived from) | National Quality Inspection (2017) 228 | Issuing agency(ies) | General Administration of Customs |
SN/T 3306.8-2017: Loop-mediated isothermal amplification detection method at frontier port--Part 8: Chikungunya virus ---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.
(State-of-the-art ring-mediated thermostatic amplification (LAMP) detection method - Part 8. Chikungunya virus)
People's Republic of China Entry-Exit Inspection and Quarantine Industry Standard
Frontier ring-mediated constant temperature amplification (LAMP) detection method
Part 8. Chikungunya virus
Part 8. Chikungunyavirus
Released on.2017-05-12
2017-12-01 implementation
People's Republic
The General Administration of Quality Supervision, Inspection and Quarantine issued
Foreword
SN/T 3306 "Land of Atmospheric Port mediated Constant Temperature Amplification (LAMP) Detection Method" is divided into 14 parts.
--- Part 1. Yersinia pestis;
--- Part 2. Toxin producing Vibrio cholerae;
--- Part 3. Shigella;
--- Part 4. Legionella pneumophila;
--- Part 5. Brucella;
--- Part 6. Yellow fever virus;
--- Part 7. Monkeypox virus;
--- Part 8. Chikungunya virus;
--- Part 9. Mycobacterium tuberculosis;
--- Part 10. Bacillus anthracis;
--- Part 11. Vibrio parahaemolyticus;
--- Part 12. Campylobacter jejuni;
--- Part 13. Plasmodium;
--- Part 14. E. coli 0157. H7.
This part is the eighth part of SN/T 3306.
This part is drafted in accordance with the rules given in GB/T 1.1-2009.
This part is proposed and managed by the National Certification and Accreditation Administration.
This section drafted by. Guangdong Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China, Guangdong International Travel Health Care Center, the Chinese people
And the National Headquarters Entry-Exit Inspection and Quarantine Bureau.
The main drafters of this section. Li Xiaobo, Li Yan, Zhu Junxian, Zhang Xianguang, Zheng Yi, Shi Yongxia, Huang Jicheng, Dai Jun, Su Jinkun.
Frontier ring-mediated constant temperature amplification (LAMP) detection method
Part 8. Chikungunya virus
1 Scope
This part of SN/T 3306 stipulates the infection of entry and exit personnel at border ports and the mosquito-mediated transmission of Chikungunya virus ring at the port.
Amplification (LAMP) nucleic acid testing procedures, including sample collection, processing, testing procedures, methods, results determination and reporting.
This section applies to laboratory rapid testing of infections of people entering and leaving the port and carrying the Chikungunya virus in mosquitoes.
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 modified versions) applies to this document.
GB 19489 General requirements for laboratory biosafety
SN/T 2300-2009 Detection method for mosquitoes carrying Chikungunya virus at border ports
SN/T 3560-2013 Multiple real-time fluorescence of yellow fever virus, dengue virus, chikungunya virus and West Nile virus at border ports
RT-PCR detection method
List of pathogenic microorganisms transmitted from humans [Weike Jiaofa (2006) No. 15]
3 Terms and definitions
The following terms and definitions apply to this document.
3.1
Chikungunya virus chikungunyavirus
A virus belonging to the genus Actinovirus of the togaviridae, whose genome is a single-strand positive-strand RNA. The virus particles are spherical, enveloped, and evenly straight.
The diameter is 42 nm, the relative molecular mass is 4.3×108, and the sedimentation coefficient is 46S. The virus can cause human Chikungunya fever, the main clinical table
It is now fever, joint pain, rash and mild bleeding.
3.2
Loop-mediated isothermal amplification assay loop-mediatedisothermalamplificationdetectionmethocl
A new method for thermostatic nucleic acid amplification, which is characterized by designing four specific primers for six regions of the target gene, using a strand replacement
The DNA polymerase can be incubated at isothermal conditions (about 63 ° C) for 30 min to 60 min to complete the nucleic acid amplification reaction. Compared with conventional PCR
The process of thermal denaturation, temperature cycling, electrophoresis, and ultraviolet observation of the template is not required.
4 Abbreviations
The following abbreviations apply to this document.
LAMP. Loop-mediated isothermal amplification
F3. LAMP reaction forward outer primer (Forwardouterprimer)
B3. LAMP reaction reverse outer primer (Backwardouterprimer)
FIP. LAMP reaction forward primer (Forwardinnerprimer)
BIP. LAMP reaction reverse internal primer (Backwardinnerprimer)
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