HOME   Cart(0)   Quotation   About-Us Policy PDFs Standard-List
www.ChineseStandard.net Database: 189759 (19 Oct 2025)

SN/T 3567.10-2017 English PDF

US$209.00 ยท In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email.
SN/T 3567.10-2017: Detection method of crossing priming isothermal amplification - Part 10: Anthracnose
Status: Valid
Standard IDContents [version]USDSTEP2[PDF] delivered inStandard Title (Description)StatusPDF
SN/T 3567.10-2017English209 Add to Cart 3 days [Need to translate] Detection method of crossing priming isothermal amplification - Part 10: Anthracnose Valid SN/T 3567.10-2017

PDF similar to SN/T 3567.10-2017


Standard similar to SN/T 3567.10-2017

GBZ 57   GB/T 31989   SN/T 3567.7   SN/T 3567.8   SN/T 3567.11   

Basic data

Standard ID SN/T 3567.10-2017 (SN/T3567.10-2017)
Description (Translated English) Detection method of crossing priming isothermal amplification - Part 10: Anthracnose
Sector / Industry Commodity Inspection Standard (Recommended)
Classification of Chinese Standard C62
Classification of International Standard 13.020
Word Count Estimation 9,929
Date of Issue 2017-07-21
Date of Implementation 2018-03-01
Quoted Standard GB/T 6682; GB 19489; SN/T 1214-2003; SN/T 2358-2009
Regulation (derived from) State-Quality-Inspection-Accreditation (2017) 337
Issuing agency(ies) General Administration of Customs
Summary This standard specifies the object, test procedure and test results of the detection of Bacillus anthracis cross-primer thermostatic amplification method at the border port. This standard is applicable to the screening test of Bacillus anthracis, and the laboratory testing of Bacillus anthracis or suspected contamination by Bacillus anthracis at the border port.

SN/T 3567.10-2017: Detection method of crossing priming isothermal amplification - Part 10: Anthracnose


---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 crossing priming isothermal amplification - Part 10. Anthracnose People's Republic of China entry and exit inspection and quarantine industry standards Cross primer constant temperature amplification detection method Part 10. Bacillus anthracis Part 10. Anthracnose Released on.2017-07-21 2018-03-01 implementation People's Republic The General Administration of Quality Supervision, Inspection and Quarantine issued

Foreword

SN/T 3567 "Cross Primer Constant Temperature Amplification Detection Method" is divided into 11 parts. --- Part 1. General technical procedures; --- Part 2. Vibrio cholerae; --- Part 3. E. coli O157.H7; --- Part 4. Yellow fever virus; --- Part 5. Salmonella; --- Part 6. Mycobacterium tuberculosis; --- Part 7. Enterovirus 71; --- Part 8. Plasmodium; --- Part 9. Yersinia pestis; ---Part 10. Bacillus anthracis; --- Part 11. Shigella. This part is the 10th part of SN/T 3567. 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. Tianjin Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China, Heilongjiang Entry-Exit Inspection and Quarantine Bureau, Hangzhou Yousida Biotechnology Co., Ltd. The main drafters of this section. Wang Xin, Yan Wendong, Zhao Hui, Yuan Jing, Li Haochen, Qi Jun, Hu Lin, especially Min. Cross primer constant temperature amplification detection method Part 10. Bacillus anthracis

1 Scope

This part of SN/T 3567 specifies the objects, detection procedures and detection procedures of the B. anthracis cross-primer constant-temperature amplification method at the border port. Report of test results. This section applies to Bacillus anthracis screening test, and infection of Bacillus anthracis or suspected Bacillus anthracis on border ports Laboratory testing of contaminated items.

2 Normative references

The 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 19489 General requirements for laboratory biosafety SN/T 1214-2003 Operational Regulations for the Treatment of Suspected Items Contaminated by Bacillus anthracis at Frontier Ports SN/T 2358-2009 Fluorescence quantitative PCR detection method for Bacillus anthracis at the border port List of pathogenic microorganisms transmitted from humans (Ministry of Health.2006)

3 Terms and definitions

The following terms and definitions apply to this document. 3.1 Cross-primer constant temperature amplification technology crossingprimingisothermalamplification; CPA A nucleic acid constant temperature amplification technology, in addition to DNA polymerase with DNA stranding function in the CPA constant temperature amplification system (DNAPoly- In addition to merase, it mainly includes cross-primers, stripping primers and detection primers. These oligonucleotide strands can rely on the DNA polymerase The highly active strand displacement property enables the cyclic amplification of deoxyribonucleic acid (DNA) to be continuously realized. 3.2 Cross primer primer Primary primer for cross-amplification, in which the 5' end sequence of the forward primer is identical to the hybridization sequence of the reverse primer, and the reverse primer The 5' end sequence is identical to the hybridization sequence of the forward primer, so the two primers are introduced into each other's hybridization sequence during amplification. Increase the hybridization site of the primer to promote the amplification reaction. 3.3 Stripping primer bumperprimer A short-stranded primer located behind the cross-amplification primer, which functions to extend the amplification primer under the action of a strand-replacement DNA polymerase The chain is peeled off from the template. 3.4 Detection primer detectionprimer A pair of short-stranded primers located inside the cross-primer, which need to be labeled with a hapten or fluorescein, so that the amplification product carries the target

Tips & Frequently Asked Questions:

Question 1: How long will the true-PDF of SN/T 3567.10-2017_English be delivered?

Answer: Upon your order, we will start to translate SN/T 3567.10-2017_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 3567.10-2017_English with my colleagues?

Answer: Yes. The purchased PDF of SN/T 3567.10-2017_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+ countries

Question 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 [email protected]. 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.