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SN/T 1087-2024 English PDF

SN/T 1087: Evolution and historical versions

Standard IDContents [version]USDSTEP2[PDF] delivered inStandard Title (Description)StatusPDF
SN/T 1087-2024EnglishRFQ ASK 3 days [Need to translate] (Technical specifications for Q fever quarantine) Valid SN/T 1087-2024
SN/T 1087-2011English419 Add to Cart 3 days [Need to translate] Quarantine protocol for Q fever Valid SN/T 1087-2011
SN/T 1087-2002English359 Add to Cart 3 days [Need to translate] Procedure of micro-complement fixation test for bovine Q fever Obsolete SN/T 1087-2002

PDF similar to SN/T 1087-2024


Standard similar to SN/T 1087-2024

GB/T 20365   SN/T 1353   NY/T 909   SN/T 1088   SN/T 1086   

Basic data

Standard ID SN/T 1087-2024 (SN/T1087-2024)
Description (Translated English) (Technical specifications for Q fever quarantine)
Sector / Industry Commodity Inspection Standard (Recommended)
Classification of Chinese Standard B41
Classification of International Standard 11.220
Date of Issue 2024-12-31
Date of Implementation 2025-07-01
Issuing agency(ies) General Administration of Customs

SN/T 1087-2011: Quarantine protocol for Q fever

---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.
Quarantine protocol for Q fever People's Republic of China Entry-Exit Inspection and Quarantine Standards Instead of the SN/T 1087-2002 Q fever quarantine Technical Specifications Issued on. 2011-05-31 2011-12-01 implementation People's Republic of China The State Administration of Quality Supervision, Inspection and Quarantine released

Foreword

This standard was drafted in accordance with GB/T 1.1-2009 given rules. Instead of the standard SN/T 1087-2002 "Q fever cattle micro complement fixation test procedures." This standard compared with SN/T 1087-2002, the main technical changes are as follows. --- Increased pathogen isolation and identification; --- Increased indirect immunofluorescence assay and enzyme-linked immunosorbent assay method. This standard is equivalent to using the World Organisation for Animal Health (OIE) "ManualofDiagnosticTestsandVaccinesfor TerrestrialAnimals "(2008 edition) the first chapter 2.1.12 Q fever section. This standard is proposed and managed by the National Certification and Accreditation Administration Committee. This standard was drafted. People's Republic of China Guangdong Entry-Exit Inspection and Quarantine Tianjin People's Republic of China Bureau, People's Republic of China Shandong CIQ. The main drafters of this standard. Yan Zhiqiang, Ke Zhongzhe, MA Bao-hua, fish Haiqiong, Lin Zhixiong, Li He, Linbao Zhen, Chen Sheng-yi, Lu Ping, LIU Ji Liang, Zhu China. This standard replaces the standards previously issued as follows. --- SN/T 1087-2002. Q fever quarantine Technical Specifications

1 Scope

This standard specifies the Q fever quarantine regulations, including pathogen isolation and identification, serological tests, including serological tests include enzyme-linked immunosorbent Attached test, indirect immunofluorescence test and complement fixation test. This standard applies to the entry and exit of cattle, sheep and other animals susceptible to Q fever quarantine and diagnosis.

2 Acronyms

The following abbreviations apply to this document. QFever. Q heat C.Burneti. Bernard Fox body Teke ELISA. enzyme-linked immunosorbent assay IFA. Indirect immunofluorescence assay HEL. human embryonic lung fibroblasts CPE. cytopathic effect PBS. phosphate buffered saline FITC. fluorescein isothiocyanate RNA. ribonucleic acid OPD. o-phenylenediamine OD values. optical density VBD. calcium and magnesium barbital buffer LPS. lipopolysaccharide

3 clinical symptoms

Q fever and other clinical information, see Appendix A.

4 quarantine methods

4.1 Isolation and Identification 4.1.1 Material preparation 4.1.1.1 Equipment. fluorescence microscope, inverted microscope, carbon dioxide incubator, 25cm2 cell culture flasks, flat-bottomed 24-well cell culture plate, Lid wet boxes, tissue masher, refrigerated centrifuge. 4.1.1.2 Reagents. 4.1.1.2.1 No C.Burnetii calf serum antibodies. 4.1.1.2.2 human embryonic lung fibroblasts (HEL).