SN/T 4853.5-2017 English PDFUS$209.00 ยท In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. SN/T 4853.5-2017: Quantitative detection of genetically modified rice. Digital PCR - Part 5: Event LL62 Status: Valid
Basic dataStandard ID: SN/T 4853.5-2017 (SN/T4853.5-2017)Description (Translated English): Quantitative detection of genetically modified rice. Digital PCR - Part 5: Event LL62 Sector / Industry: Commodity Inspection Standard (Recommended) Classification of Chinese Standard: X11 Word Count Estimation: 9,945 Date of Issue: 2017-07-21 Date of Implementation: 2018-03-01 Regulation (derived from): National Quality Inspection (2017) No. 337 Issuing agency(ies): General Administration of Customs SN/T 4853.5-2017: Quantitative detection of genetically modified rice. Digital PCR - Part 5: Event LL62---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. (Quantitative Detection of Transgenic Rice by Digital PCR Method Part 5. LL62 Lines) People's Republic of China entry and exit inspection and quarantine industry standards GM rice quantitative detection digital PCR Part 5. LL62 strain Part 5. EventLL62 Released on.2017-07-21 2018-03-01 implementation People's Republic The General Administration of Quality Supervision, Inspection and Quarantine issued ForewordSN/T 4853 "GMO quantitative detection digital PCR method" series of standards are divided into 7 parts. --- Part 1. TT51-1 strain; --- Part 2. Kezhen rice line; --- Part 3. Kefeng No. 6 strain; --- Part 4. M12 strain; --- Part 5. LL62 strain; --- Part 6. T2A-1 strain; --- Part 7. T1C-19 strain. This part is the fifth part of the SN/T 4853 standard. This part is drafted in accordance with the rules given in GB/T 1.1-2009. Please note that some of the contents of this document may involve patents. The issuing organization of this document is not responsible for identifying these patents. This part is proposed and managed by the National Certification and Accreditation Administration. This section drafted by. China Academy of Inspection and Quarantine, Shanghai Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China. The main drafters of this section. Li Xiang, Ren Yifei, Li Xiaohong, Huang Wensheng, Deng Tingting, Chen Ying, Pan Liangwen. GM rice quantitative detection digital PCR Part 5. LL62 strain1 ScopeThis standard specifies the digital PCR quantitative detection method for LL62 strain in rice and rice. This standard applies to digital PCR quantitative detection of LL62 strain specificity in rice and rice. The method has a quantitative detection limit (LOQ) of 0.1% (mass fraction).2 Normative referencesThe following documents are indispensable for the application of this document. For dated references, only the dated version applies to this article. Pieces. For undated references, the latest edition (including all amendments) applies to this document. GB/T 6682 Analytical laboratory water specifications and test methods GB/T 19495.1 General requirements and definitions for the detection of genetically modified products GB/T 19495.2 Technical requirements for testing laboratory of genetically modified products GB/T 19495.3 Transgenic product detection nucleic acid extraction and purification method GB/T 19495.5 Genetically modified nucleic acid quantitative PCR detection method for genetically modified products GB/T 19495.7 GM product testing sampling and sample preparation method SN/T 1194 Detection and sampling method for genetically modified components of plants and their products 3 Terms, definitions and abbreviations 3.1 Terms and definitions The following terms and definitions apply to this document. 3.1.1 SPS gene Thegeneofsucrosephosphatesynthase Sucrose phosphate synthase gene, rice single copy internal reference gene. 3.1.2 LL62 transformant specific sequence event-specificsequenceofLL62 The contiguous region sequence resulting from the recombination of the foreign DNA into the recipient rice genome. See Appendix A for specific sequences. 3.1.3 Taq enzyme TaqDNApolymerase A thermostable DNA polymerase derived from Azotobacter. 3.1.4 Template template Specific DNA fragments detected by digital PCR primer/probe amplification. 3.1.5 Quantitative detection of low limit limitofquantification; LOQ The percentage of the lowest transgenic component that can be quantified by the assay under conditions of a relative standard deviation of no more than 25%. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of SN/T 4853.5-2017_English be delivered?Answer: Upon your order, we will start to translate SN/T 4853.5-2017_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. The lengthier the document the longer the lead time.Question 2: Can I share the purchased PDF of SN/T 4853.5-2017_English with my colleagues?Answer: Yes. The purchased PDF of SN/T 4853.5-2017_English will be deemed to be sold to your employer/organization who actually pays for it, including your colleagues and your employer's intranet.Question 3: Does the price include tax/VAT?Answer: Yes. Our tax invoice, downloaded/delivered in 9 seconds, includes all tax/VAT and complies with 100+ countries' tax regulations (tax exempted in 100+ countries) -- See Avoidance of Double Taxation Agreements (DTAs): List of DTAs signed between Singapore and 100+ countriesQuestion 4: Do you accept my currency other than USD?Answer: Yes. If you need your currency to be printed on the invoice, please write an email to Sales@ChineseStandard.net. In 2 working-hours, we will create a special link for you to pay in any currencies. Otherwise, follow the normal steps: Add to Cart -- Checkout -- Select your currency to pay. |