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potato virus x quarantine identification method background detection result specifications purpose detection sensitivity microplate reader micro-volume detection potato virus x introduction national standard potato virus x offset rubber blanket standard technical moduleskey emulsion wastewater
GB/T 36833-2018 in English

GB/T 36833-2018 in English

VALID

Detection and identification of Potato virus X

  • 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 36833-2018
Document status: VALID
Title in English: Detection and identification of Potato virus X
Title in Chinese: 马铃薯X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: potato virus x quarantine identification method background
detection result
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《GB/T 36833-2018马铃薯X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

National Standard of the People's Republic of China GB/T 36833—2018

Potato virus X quarantine identification method

Background and significance of standard formulation

The formulation of GB/T 36833—2018 is based on the important position of potato in international trade and agricultural production. Potato virus X (PVX) is a quarantine disease that seriously affects potato yield and quality. The introduction of this standard fills the gap in the field of PVX detection methods in China, and provides a scientific basis for standardizing import and export plant quarantine and ensuring agricultural safety.


Detection principle and technical route

The genomic characteristics and immunogenicity of PVX are the main basis for its quarantine identification. The standard adopts a variety of molecular biology techniques and immunological methods, including:

  • Reverse transcription PCR (RT-PCR)
  • Real-time fluorescence reverse transcription PCR (Real-time RT-PCR)
  • Reverse transcription loop-mediated isothermal amplification (RT-LAMP)
  • Enzyme-linked immunosorbent assay (ELISA)
  • Immunochromatographic test strip test
  • Dot enzyme-linked immunosorbent assay (dot-ELISA)

Main instruments and equipment and function comparison table

Instrument name Model and specifications Purpose Detection sensitivity
Microplate reader Micro-volume detection, suitable for ELISA and dot-ELISA Optical density (OD) determination, sensitivity up to 0.001
PCR instrument Variable temperature control, support gradient PCR DNA amplification, suitable for RT-PCR and Real-time RT-PCR Single copy detection level
Real-time fluorescence PCR instrument Equipped with fluorescence detection module Quantitative analysis of viral load, Ct value range: 15-40 Ct ≤ 35 is positive
RT-LAMP detector Constant temperature amplification, 65℃ Rapid nucleic acid amplification, suitable for on-site detection Colorimetric reaction to directly determine the result

Sample preparation and sampling methods

The standard specifies a detailed sample preparation process, including:

  1. Cultivation and observation of tissue culture seedlings, miniature potatoes, and tubers
  2. Sowing and symptom monitoring of host plant seeds of the Solanaceae family
  3. Direct detection of samples with suspicious symptoms

Result determination and record keeping

The detection result is determined by a double confirmation mechanism:

  • Negative samples must be negative by at least one method
  • Positive samples must be positive by at least two methods

Implementation suggestions and precautions

In order to ensure the effective implementation of the standard, the following suggestions are put forward:

  1. Laboratory conditions:Equipped with Class II biosafety protection facilities.
  2. Staff training:Regularly conduct training on testing methods and quality control.
  3. Reagent management:Establish a reagent validity period and traceability record system.
  4. Data sharing:Promote the information management and sharing mechanism of quarantine results.

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