GB/T 19495.9-2017 in English
VALIDDetection of genetically modified organisms and derived products―Liquid bead array detection for plant products
- Issued on:-
- Implemented on:2018-07-01
- File Format:PDF
- Delivery:Via email within 1~3 business days
$97.00
《GB/T 19495.9-2017转基因产品检测 植物产品液相芯片检测方法》由TC387(全国生化检测标准化技术委员会)归口,主管部门为国家标准化管理委员会。
Introduction
GB/T 19495.9—2017 In-depth interpretation of liquid phase chip detection methods for genetically modified products
Background and significance of the standard
The rapid development of genetically modified technology has promoted changes in the global agriculture and food industry, and has also brought about important needs for the detection of genetically modified ingredients. As an important part of China's national standards, GB/T 19495.9—2017 aims to provide scientific and standardized methods for the qualitative detection of genetically modified ingredients in plants and their products.
This standard focuses on liquid phase chip technology, which is an efficient, sensitive and high-throughput detection method. Through fluorescently encoded microspheres and flow cytometry, multiple target DNA sequences can be quickly identified and quantified. This method has significant advantages in the field of genetically modified detection, especially in large-scale sample screening.
Comparative Analysis of Standard Frameworks
| Standard Number | Scope of Application | Detection Method | Main Features |
|---|---|---|---|
| GB/T 19495.1 | General Requirements and Definitions for Detection of Genetically Modified Products | Basic Framework and Terminology Specifications | Laying the Foundation for the Standard System |
| GB/T 19495.6 | Gene Chip Detection Method for Detection of Genetically Modified Products | Detection Technology Based on Solid Phase Chip | High-throughput, Multi-target Detection |
| GB/T 19495.9 | Liquid-phase chip detection method for plant products | Fluorescence detection technology based on liquid-phase microspheres | High sensitivity and rapid screening |
Working principle of liquid-phase chip technology
The core of liquid-phase chip technology lies in the preparation and detection of fluorescent-encoded microspheres. Each microsphere has a specific probe on its surface for capturing the target DNA sequence. The spectroscopic fingerprint of the microsphere and the bound reporter molecule are detected by red and green lasers, respectively, to achieve qualitative and quantitative analysis.
The following are the key steps of liquid-phase chip detection:
- DNA extraction and preparation: According to the standard requirements, use the kit to extract the DNA in the target sample and ensure its purity and concentration.
- PCR amplification: Amplify the target gene fragment, including the endogenous control gene (18s rRNA) and the exogenous screening element (CaMV35S promoter and NOS terminator) through polymerase chain reaction (PCR).
- Hybridization reaction: Combine the PCR product with the specific probe in the liquid phase chip to form a stable hybrid chain.
- Fluorescence detection: Detect the fluorescence signal of the microspheres by flow cytometry, and analyze the median fluorescence intensity (MFI) to determine the presence or absence of the target gene.
Implementation recommendations and precautions
Case study: Detection of genetically modified corn
In actual application, a testing agency used this standard to conduct liquid phase chip testing on a batch of imported genetically modified corn samples. The positive results of endogenous genes (18s rRNA) and the positive signals of exogenous screening elements (CaMV35S) confirmed that the samples contained genetically modified components. The detection sensitivity reached 0.01%, which meets the international standards.
This case shows that:
- Strictly following standard operating procedures is the key to ensuring detection accuracy.
- The setting of positive controls and negative controls helps to exclude false positive and false negative results.
- Liquid phase chip technology has significant advantages in high-throughput detection and is suitable for large-scale sample screening.

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