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triple rt-pcr detection method local standards detection technology triple rt-pcr multiplex pcr high compatibility operation triplex rt-pcr assay grass carp reovirus grass carp neutron detection methods radiometric calibration method internal combustion generator shaft systems
GB/T 37746-2019 in English

GB/T 37746-2019 in English

VALID

Triplex RT-PCR assay for detection of grass carp reoviruses

  • Issued on:2019-06-04
  • Implemented on:2020-01-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $220.00
$214.00
Standard No: GB/T 37746-2019
Document status: VALID
Title in English: Triplex RT-PCR assay for detection of grass carp reoviruses
Title in Chinese: 草鱼呼肠孤病毒三重RT-PCR检测方法
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 business days
Issued on: 2019-06-04
Implemented on: 2020-01-01
ICS Classification: 65.020.30-Animal husbandry and breeding
Chinese Classification: B41-Animal quarantine, veterinary and epidemic prevention
Professional Classification: GB-National Standard
Related Keywords: triple rt-pcr detection method
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grass carp reovirus
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《GB/T 37746-2019草鱼呼肠孤病毒三重RT-PCR检测方法》由TC156(全国水产标准化技术委员会)归口,TC156SC11(全国水产标准化技术委员会水产养殖病害防治分会)执行,主管部门为农业农村部。


Introduction

1. Background and significance of the standard

GB/T 37746—2019 is a standard of the Technical Committee for Aquatic Products Standardization proposed by the Ministry of Agriculture and Rural Affairs of the People's Republic of China, mainly for the triple RT-PCR detection method of grass carp reovirus (GCRV). The formulation of this standard fills the gap in the field of fish reovirus detection in my country and provides a scientific basis for the prevention and control of aquatic animal diseases.

2. Comparison of standard frameworks

Standard dimensions GB/T 37746—2019 International reference standard Comparison of local standards
Detection scope Three genotypes of grass carp reovirus (I, II, III) Covering a variety of aquatic animal viruses Complementary to local standards
Detection technology Triple RT-PCR Multiplex PCR High compatibility
Operation steps One-step method and two-step method Traditional step-by-step method Significantly improved efficiency

3. Technical principles and reagent requirements

Technical principles:By designing specific primers for different genotypes of GCRV, three nucleic acid fragments of different sizes are amplified in the same PCR reaction system and distinguished by agarose gel electrophoresis.

Reagents and materials

  • M-MLV reverse transcriptase:Key enzyme for cDNA synthesis, needs to be stored at -20°C.
  • dNTPs:Contains 10mmol/L each of dCTP, dATP, dGTP, and dTTP.
  • Taq DNA polymerase:Used for PCR amplification, needs to be stored at -20°C.

4. Implementation Suggestions

To ensure the accuracy and consistency of the test, the following suggestions are made:
1. The testing agency should be equipped with PCR equipment and electrophoresis systems that meet the standard requirements.
2. The reagents must be sterilized in strict accordance with the standard requirements.
3. The operators must receive professional training and master the RT-PCR technology.

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