SN/T 3330-2012Protocol of identification for Tachypleus tridentatus. PCR method (English PDF)
中国鲎物种鉴定方法 PCR方法
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Issued by
General Administration of Customs
Level / Type
National · Recommended
Issue date
December 12, 2012
Implementation date
July 1, 2013
Scope
SN/T 3330-2012 is the English-translated version of 中国鲎物种鉴定方法 PCR方法.
SN/T 3330-2012 - This standard specifies the Chinese horseshoe crab species by PCR method. This standard applies to entry and exit aquatic and biological preparations containing Chinese horseshoe crab ingredient identification of Chinese horseshoe crab.
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Document preview — SN/T 3330-2012
National Standard of the People's Republic of China
Issued by: General Administration of Customs
Contents
- Foreword
- 1 Scope
- 2 Normative references
- 3 Terms and Definitions
- 5 Equipment and Reagents
- 5.1 Equipment
- 5.2 Reagents
Foreword
This standard was drafted in accordance with GB/T 1.1-2009 given rules.
Please note that some of the content of this document may involve patents. Distribution of this document Structure does not bear the responsibility to identify these patents.
This standard is proposed and managed by the National Certification and Accreditation Administration Committee.
This standard was drafted. People's Republic of China Yantai Exit Inspection and Quarantine, People's Republic of China Shandong Entry-Exit Inspection and Quarantine Bureau.
1 Scope
This standard specifies the Chinese horseshoe crab species by PCR method.
This standard applies to entry and exit aquatic and biological preparations containing Chinese horseshoe crab ingredient identification of Chinese horseshoe crab.
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. For undated references, the latest edition (including any amendments) applies to this document.
Laboratory use specifications and test methods GB/T 6682 Analysis SN/T 1193 genetic testing laboratory technical requirements
3 Terms and Definitions
The following terms and definitions apply to this document.
Polymerase chain reaction polymernasechainreaction; PCR in thermostable DNA polymerase and a pair of primers (tested with target nucleic acid molecule sequences homologous DNA fragments) at high temperature (DNA points Sub-denatured) and low temperature (primer profit target nucleic acid molecule complex nature and thermostable DNA polymerase extension) alternating cycles of amplification of the target nucleic acid test Child approach.
Principle 4
Chinese horseshoe crab (morphological characteristics see Appendix A) sample after extraction of total genomic DNA, the use of specific primers designed by conventional PCR specific amplification technology Chinese horseshoe crab mtDNACOX3 gene fragment (349bp). Chinese horseshoe crab samples is determined according to the results of PCR amplification is Chinese horseshoe crab species. Specific primers by mtDNA than Chinese horseshoe crab, Limulus round tail, American horseshoe crab, Limulus and other mostly southern horseshoe crab COX3 gene fragments designed.
5 Equipment and Reagents
5.1 Equipment
PCR, tissue grinder, clean table, ice maker, high-speed refrigerated centrifuge, water bath, small desktop centrifuge, a conventional refrigerator, Vortex, electrophoresis, gel imaging system.
5.2 Reagents
Unless otherwise specified, all reagents were of analytical grade.
5.2.1 Water. should be consistent with GB/T 6682 in a water specifications. For PCR (including nucleic acid extraction) are used when water with DEPC at Treated to remove RNA enzyme.
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This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 7 pages — is available in the English PDF.
Referenced standards
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Related Standards
GB/T 6682-1992 — Water for analytical laboratory use--Specification and test methods
GB/T 6682-2008 — Water for analytical laboratory use - Specification and test methods
SN/T 1193-2003 — General requirements for the laboratories for gene detection and identification
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SN/T 3330-2012
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