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SN/T 4793-2017 English PDF

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SN/T 4793-2017: Test methods for Plasmodium by real time PCR at ports
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PDF similar to SN/T 4793-2017


Standard similar to SN/T 4793-2017

GBZ 57   GB/T 31989   SN/T 5800.2   SN/T 5800.1   SN/T 4794   

Basic data

Standard ID SN/T 4793-2017 (SN/T4793-2017)
Description (Translated English) Test methods for Plasmodium by real time PCR at ports
Sector / Industry Commodity Inspection Standard (Recommended)
Classification of Chinese Standard C62
Word Count Estimation 10,169
Date of Issue 2017-05-12
Date of Implementation 2017-12-01
Regulation (derived from) State-Quality-Inspection-Accreditation (2017) 228
Issuing agency(ies) General Administration of Customs

SN/T 4793-2017: Test methods for Plasmodium by real time PCR at ports

---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 of Plasmodium falciparum by Real - time Fluorescence) People's Republic of China Entry-Exit Inspection and Quarantine Industry Standard Real-time fluorescent PCR detection method for malaria parasites at border ports Released on.2017-05-12 2017-12-01 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 is proposed and managed by the National Certification and Accreditation Administration. This standard was drafted. Guangdong Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China, Shantou Entry-Exit Inspection and Quarantine Bureau, Guangzhou Airport Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China. The main drafters of this standard. Shi Yongxia, Li Xiaobo, Zhu Junxian, Li Yan, Huang Jicheng, Xing Luqin, Hong Wei, Sun Wei, Zhong Yuqing, Xiang Dapeng. Real-time fluorescent PCR detection method for malaria parasites at border ports

1 Scope

This standard specifies the biosafety requirements for malaria detection at border ports, the collection, transportation and preservation of specimens, and real-time fluorescent PCR for malaria. Test method. This standard is applicable to real-time fluorescent PCR of suspected falciparum malaria, vivax malaria, ovarian malaria and three-day malaria infected persons at border ports. Detection.

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 19489 General requirements for laboratory biosafety 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 Malaria malaria Parasitic diseases caused by human Plasmodium infection are mainly transmitted by female Anopheles bites. Plasmodium first invades liver cells to develop and reproduce, and then Invasion of red blood cells to breed, causing red blood cells to burst and disease. Clinically, after repeated episodes of intermittent chills, high fever, followed by sweating Mitigation is characteristic. 3.2 Plasmodium Plasmodium It belongs to Eucoccidida, Plasmodidae, Plasmodium, and is the causative agent of malaria. body. There are four species of parasitic parasites in humans, namely Plasmodiumvivax and Plasmodiumfalci- Parum), Plasmodium malariae and Plasmodiumovale, causing vivax malaria Sexual malaria, three-day malaria and oval malaria.

4 Abbreviations

The following abbreviations apply to this document. Real-time fluorescent RT-PCR. real-time fluorescent reverse transcription-polymerase chain reaction. Ct value. The number of cycles experienced when the fluorescent signal in each reaction tube reaches a set threshold. DNA. Deoxyribonucleic acid. FAM. FAM fluorescent dye, a fluorescent reporter group.

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