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GB/T 36752-2018 in English

GB/T 36752-2018 in English

VALID

Detection and identification of Sowbane mosaic virus

  • Issued on:2018-09-17
  • Implemented on:2019-04-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $220.00
$214.00
Standard No: GB/T 36752-2018
Document status: VALID
Title in English: Detection and identification of Sowbane mosaic virus
Title in Chinese: 藜草花叶病毒检疫鉴定方法
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 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: sowbane mosaic virus
chenopodium album mosaic virus
international standards detection
detection principle
detection methods choose
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《GB/T 36752-2018藜草花叶病毒检疫鉴定方法》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

1. Background and significance of standard formulation

GB/T 36752-2018 "Quarantine and identification methods for Chenopodium album mosaic virus" is a domestic standard formulated according to international plant quarantine standards, aiming to standardize the detection process of Chenopodium album mosaic virus (Sowbane mosaic virus, SoMV). The virus is mainly transmitted mechanically and through seeds, and harms a variety of economic crops and fruit trees.

2. Comparison of standard frameworks

Standard dimensions GB/T 36752—2018 Differences in international standards
Detection method DAS-ELISA, RT-PCR, real-time fluorescence RT-PCR In line with international standards, using advanced molecular biology technology
Scope of application Plant seeds, seedlings and products Covering major economic crops and fruit trees
Detection sensitivity Can detect trace amounts of viruses Reaching the international advanced level

3. Detection principle and technical path

Detection principle: Based on the serological characteristics and genomic characteristics of the virus, multiple methods are used for joint detection. Specifically including:

  • DAS-ELISA: Double antibody sandwich enzyme-linked immunosorbent assay
  • RT-PCR: Reverse transcription polymerase chain reaction
  • Real-time fluorescence RT-PCR: Real-time monitoring of virus amplification

4. Implementation suggestions

4.1 Preparation and preservation of test samples

Seed samples should be selected from deformed seeds or plants showing symptoms, and seedlings and plant products should be sampled in accordance with SN/T 2122. Test samples need to be stored at different temperatures: 4℃ for seeds, -80℃ for seedlings and leaves, for review.

4.2 Selection of detection methods

Choose an appropriate combination of methods according to the detection requirements. For suspected samples, it is recommended to perform DAS-ELISA and RT-PCR tests at the same time to improve accuracy.

4.3 Recording and reporting of results

Record the sample source, detection time, method and results in detail. Enzyme-linked reaction values, electrophoresis images and fluorescence curves should be saved as important attachments.

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