GA 471-2004 English PDF

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GA 471-2004: Serum products of anti-A, anti-B antibodies
Status: Obsolete

Standard ID	USD	BUY PDF	Lead-Days	Standard Title (Description)	Status
GA 471-2004	279	Add to Cart	3 days	Serum products of anti-A, anti-B antibodies	Obsolete

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Basic data

Standard ID: GA 471-2004 (GA471-2004)
Description (Translated English): Serum products of anti-A, anti-B antibodies
Sector / Industry: Public Security (Police) Industry Standard
Classification of Chinese Standard: A92
Classification of International Standard: 13.310
Word Count Estimation: 7,772
Date of Issue: 2004-03-16
Date of Implementation: 2004-07-01
Quoted Standard: GB/T 2828.1-2003
Summary: This standard specifies the quality requirements, testing methods and testing rules of anti-A and anti-B serum reagents used in forensic biological samples. This standard is applicable to the production, inspection and trade of anti-A and anti-B serum reagents used in forensic biological sample ABO blood type identification.

GA 471-2004: Serum products of anti-A, anti-B antibodies

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Serum products of anti-A, anti-B antibodies ICS 13.310 A92 People's Republic of China Public Safety Industry Standard anti-A, anti-B serum reagent Released on.2004-03-16 2004-07-01 implementation Ministry of Public Security

Content

Foreword III 1 Scope 1 2 Normative references 1 3 Terms and Definitions 1 4 reagent classification 1 5 Quality requirements 1 6 pathogenic microorganism detection 2 7 Marking, packaging, transportation, storage 2 8 Detection method 2 9 Detection rules 4

Foreword

The full technical content of this standard is mandatory. This standard is proposed and managed by the National Criminal Technology Standardization Committee. This standard was drafted. Ministry of Public Security Material Identification Center. Drafters of this standard. Wen Peizhong, Cheng Weiwei, Xie Qun, Zhang Chunhuan, Zhang Haibing, Li Zhaolong, Zhang Yinglan, and Ying Yingsong. anti-A, anti-B serum reagent

1 Scope

This standard specifies the quality requirements, testing methods and testing rules for anti-A and anti-B serum reagents used in the examination of medical doctor samples. This standard is applicable to the production, testing and trade of anti-A and anti-B serum reagents for the ABO blood type identification of legal doctor samples.

2 Normative references

The terms in the following documents become the terms of this standard by reference to this standard. All dated references, followed by all Modifications (not including errata content) or revisions do not apply to this standard, however, parties to agreements based on this standard are encouraged to study Is it possible to use the latest version of these files? For undated references, the latest edition applies to this standard. GB/T 2828.1-2003 - Sampling procedures for sampling by sampling - Part 1 Plan (ISO 2859-1.1999, IDT)

3 Terms and definitions

This standard uses the following terms and definitions. 3.1 A reagent for detecting ABO blood type of biological samples such as human blood (spot), body fluid (spot), hair, bone, and the like. Simultaneous detection of both reagents A sample can be preliminarily determined that its ABO blood type is A type, B type, AB type or O type.

4 reagent classification

4.1 Classification by type of preparation 4.1.1 Lyophilization reagent. 4.1.2 Liquid reagents. 4.2 Classification by reagent source 4.2.1 Human anti-A, anti-B serum reagents. 4.2.2 Anti-A, anti-B serum reagents.

5 Quality requirements

5.1 Appearance characteristics 5.1.1 After the addition of the indicator, the anti-A serum reagent is a blue transparent liquid, and the anti-B serum reagent is a yellow or red transparent liquid. 5.1.2 After adding the indicator, the lyophilized anti-A serum reagent is blue loose body, and the anti-B serum reagent is yellow or red loose body, and the standard is added. After dissolving the solution, it should be completely dissolved into blue and yellow or red transparent liquid within 2 min. 5.2 Agglutination titer Anti-A serum reagent and anti-B serum reagent should be greater than or equal to 128 times within 60 min. 5.3 Specificity Within 60 min, the specificity should meet the requirements of Table 1. ......

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