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SN/T 1181.2-2003 English PDF

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SN/T 1181.2-2003: Detection antibodies against foot and mouth disease virus. Protocol of micro-serum neutralization test
Status: Obsolete
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SN/T 1181.2-2003English319 Add to Cart 3 days [Need to translate] Detection antibodies against foot and mouth disease virus. Protocol of micro-serum neutralization test Obsolete SN/T 1181.2-2003

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Basic data

Standard ID SN/T 1181.2-2003 (SN/T1181.2-2003)
Description (Translated English) Detection antibodies against foot and mouth disease virus. Protocol of micro-serum neutralization test
Sector / Industry Commodity Inspection Standard (Recommended)
Classification of Chinese Standard B41
Word Count Estimation 8,859
Date of Issue 2003-03-17
Date of Implementation 2003-09-01
Adopted Standard OIE 2.1.1-2000; NEQ
Regulation (derived from) State inspection recognized [2010] No. 582
Issuing agency(ies) General Administration of Quality Supervision, Inspection and Quarantine of the People Republic of China

SN/T 1181.2-2003: Detection antibodies against foot and mouth disease virus. Protocol of micro-serum neutralization test


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Detection antibodies against foot and mouth disease virus.Protocol of micro-serum neutralization test Book of the People's Republic of China Entry and Exit Inspection and Quarantine Foot and mouth disease virus antibody detection method Trace serum neutralization test Released on.2003-03-17 2003-09-01 implementation People's Republic The General Administration of Quality Supervision, Inspection and Quarantine issued

Foreword

This standard was drafted in accordance with the relevant content of the OIE Diagnostic Test and Vaccine Standards Manual, Chapter 4, Chapter 2.1.1 of.2000. Appendix A and Appendix B of this standard are standard informative annexes. This standard is proposed and managed by the National Certification and Accreditation Administration. This standard was drafted. Zhuhai Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China. The main drafters of this standard. Yang Su, Xue Jingshan, Lu Hong, Feng Jiawang. This standard is the industry standard for inspection and quarantine issued for the first time. Foot-and-mouth disease virus antibody detection method, trace serum neutralization test

1 Scope

This standard specifies the test method for the neutralization of foot-and-mouth disease virus. This standard applies to the detection of neutralizing antibody levels of foot-and-mouth disease virus.

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 6682-1992 "Analysis laboratory water specifications and test methods"

3 Abbreviations

The following abbreviations apply to this standard. 3.1 CPE Caused by cytopathic effects. 3.2 TCID50 Half of the amount of cell infection. 3.3 FMD Foot and mouth disease.

4 Principle

The specific serum neutralizing antibody binds to the virus, which can make the virus lose its ability to infect sensitive cells, thus preventing the virus from spreading. Colonization. This reaction is manifested not only as a virus can only be neutralized by the corresponding immune serum, but also in neutralizing a certain amount of virus, Must have a certain titer of immune serum. The neutralization test specified in this standard is based on quantitative virus dilution serum, when serum can prevent quantification When the virus is 50% cytopathogenic, its serum dilution is its potency. Therefore, the neutralization test is a quantitative determination of foot-and-mouth disease blood. The method of clearing antibodies.

5 reagents and materials

5.1 The water used in this standard shall comply with the specifications for tertiary water (three distilled water) in GB/T 6682-1992. 5.2 Refer to Appendix A for the reagent formulations used in this standard. 5.3 Unless otherwise specified, all reagents in this standard refer to analytical reagents. 5.4 Reagents and glassware used in this standard are autoclaved except for special regulations. 5.5 Virus O, A, C, SAT1, SAT2, SAT3 and AsiaI type foot-and-mouth disease cytotoxicity purified by plaque method and serologically identified As the standard toxicity for each type of serum antibody detection.

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