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GB/T 34738-2017 English PDF

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GB/T 34738-2017: Method of the real-time PCR for the detection of honeybees sacbrood disease
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PDF similar to GB/T 34738-2017


Standard similar to GB/T 34738-2017

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Basic data

Standard ID GB/T 34738-2017 (GB/T34738-2017)
Description (Translated English) Method of the real-time PCR for the detection of honeybees sacbrood disease
Sector / Industry National Standard (Recommended)
Classification of Chinese Standard B41
Classification of International Standard 11.220
Word Count Estimation 12,145
Date of Issue 2017-11-01
Date of Implementation 2018-05-01
Regulation (derived from) National Standard Announcement 2017 No. 29
Issuing agency(ies) General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China

GB/T 34738-2017: Method of the real-time PCR for the detection of honeybees sacbrood disease

---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.
Method of the real-time PCR for the detection of honey bees sacbrood disease ICS 11.220 B41 National Standards of People's Republic of China Fluorescent PCR Detection of Honeybee Cysticercosis Posted.2017-11-01 2018-05-01 implementation General Administration of Quality Supervision, Inspection and Quarantine of People's Republic of China China National Standardization Administration released

Foreword

This standard was drafted in accordance with the rules given in GB/T 1.1-2009. This standard proposed by the People's Republic of China Ministry of Agriculture. This standard by the National Animal Husbandry Standardization Technical Committee (SAC/TC181) centralized. This standard was drafted unit Jilin Entry-Exit Inspection and Quarantine of People's Republic of China, Jilin University, People's Republic of China Fujian Entry and Exit Inspection and Quarantine Bureau. The drafters of this standard. Song war Yun, Feng Xin, Meng Rising, Liu Jinhua, Wei Chunyan, Mu Jun, Wang Zhenguo, Zheng Teng, Meng Qingfeng, Cai Yang, Xiao Cheng Rui, Wang Weili. Fluorescent PCR Detection of Honeybee Cysticercosis

1 Scope

This standard specifies the bee larvae cytoplasmic fluorescence PCR detection method. This standard applies to bees and larvae in cystic larval disease detection.

2 Normative references

The following documents for the application of this document is essential. 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 18088 exit quarantine animal samples

3 Reagents and materials

Unless otherwise specified, only analytical reagents are used. All reagents were treated with RNase-free containers (treated with diethyl pyrocarbonate After autoclave) dispensing. 3.1 water, GB/T 6682, three. 3.2 bee larvae virus. 3.3 Primers and Probes, Upstream Primer F1 (10 pmol/μL) .5'-AAGTTGGAGGCGCGYATTTG-3 ', Downstream Primer R1 (10 pmol/μL) .5'-CAAATGTCTTCTTACDAGAAGYAAGGATTG-3 ', probe P1 (5 pmol/μL). 5'-FAM-CGGAGTGGAAAGAT-TAMRA-3 '. 3.4 phosphate buffered saline, the preparation method see A.1. 3.5 Total RNA extraction reagent. 3.6 chloroform. 3.7 isopropanol. 3.8 75% ethanol. Note. Prepare with freshly opened absolute ethanol and diethyl pyrocarbonate. 3.9 Coke-diethyl carbonate treated water. 3.10 reverse transcriptase. 3.11 RNase inhibitor (40U/μL). 3.12 5 × reverse transcriptase buffer. 3.13 10 × PCR reaction buffer (containing magnesium ions). 3.14 DNA Polymerase (5U/μL). 3.15 Deoxyribonucleotide triphosphates (dNPTs 10 mmol/L each).

4 equipment

4.1 fluorescence quantitative PCR amplification instrument.

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