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method detection method principle scope detection sensitivity rapid qualitative detection rt-pcr reverse transcription polymerase chain reaction specificity detection standard frameworks detection method advantages disadvantages das-elisa easy ultraviolet spectrophotometric method scopethis standard chemical solid material transfer pumps introductionthis document artificial short-rotation
GB/T 36816-2018 in English

GB/T 36816-2018 in English

VALID

Detection and identification of Potato virus Y

  • Issued on:2018-09-17
  • Implemented on:2019-04-01
  • File Format:PDF
  • Delivery:Via email within 5 business days
Price(USD): $310.00
$301.00
Standard No: GB/T 36816-2018
Document status: VALID
Title in English: Detection and identification of Potato virus Y
Title in Chinese: 马铃薯Y病毒检疫鉴定方法
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 5 business days
Issued on: 2018-09-17
Implemented on: 2019-04-01
ICS Classification: 65.020.01-Farming and forestry in general
Chinese Classification: B16-Plant quarantine, pest control
Professional Classification: GB-National Standard
Related Keywords: method detection method principle scope
detection sensitivity
rapid qualitative detection rt-pcr reverse transcription polymerase chain reaction
specificity detection
standard frameworks detection method advantages disadvantages das-elisa easy
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《GB/T 36816-2018马铃薯Y病毒检疫鉴定方法》由TC271(全国植物检疫标准化技术委员会)归口,主管部门为国家标准化管理委员会。


Introduction

GB/T 36816—2018 Standard Overview

This standard specifies in detail the quarantine identification methods for Potatovirus Y (PVY), and is applicable to potato plants, propagation materials and other host plants that may carry the virus.

Background of Standard Formulation

Potatovirus Y is a quarantine disease of global concern, and its transmission pathways are diverse, including asexual propagation materials and mechanical inoculation. This standard was proposed by the National Technical Committee for Plant Quarantine Standardization and aims to provide unified technical specifications for domestic and international trade.

Principle and technical framework of the method

Detection method Principle Scope of application
DAS-ELISA Immunological method based on antigen-antibody reaction Suitable for rapid qualitative detection
RT-PCR Reverse transcription polymerase chain reaction, based on viral genome characteristics Suitable for high sensitivity and specificity detection
Real-time RT-PCR Real-time quantitative reverse transcription polymerase chain reaction, combined with fluorescent labeling Used for quantitative analysis of viral load

Comparison of standard frameworks

RT-PCR
Detection method Advantages Disadvantages
DAS-ELISA Easy to operate and low cost Low sensitivity, requires high-quality reagents
RT-PCR High sensitivity and specificity Complex operation and long cycle
Real-time quantitative reverse transcription polymerase chain reaction, combined with fluorescent labeling Used for quantitative analysis of viral load
Real-time monitoring, quantitative analysis Highly equipment-dependent

Implementation recommendations

Reagent selection:Preferably use validated commercial kits to ensure detection sensitivity and specificity.

Sample processing:Strictly follow standard requirements for sample sampling and preparation to avoid contamination and operational errors.

Data recording:Record the experimental process and results in detail to ensure data traceability and integrity.

Sample only — not a preview of GB/T 36816-2018
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