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Position: Chinese Standard in English/GB/T 14926.24-2026
GB/T 14926.24-2026   Laboratory animal—Method for examination of pneumonia virus of mice (PVM) (English Version)
Standard No.: GB/T 14926.24-2026 Status:to be valid remind me the status change

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Target Language:English File Format:PDF
Word Count: 7500 words Translation Price(USD):225.0 remind me the price change

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Implemented on:2026-5-1 Delivery: via email in 1~3 business day

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,,2026-5-1,1E3E791C3BFD555B1770337762875
Standard No.: GB/T 14926.24-2026
English Name: Laboratory animal—Method for examination of pneumonia virus of mice (PVM)
Chinese Name: 实验动物 小鼠肺炎病毒检测方法
Chinese Classification: B44    Domesticate animal
Professional Classification: GB    National Standard
ICS Classification: 65.020.30 65.020.30    Animal husbandry and breeding 65.020.30
Source Content Issued by: SAMR, SAC
Issued on: 2026-01-28
Implemented on: 2026-5-1
Status: to be valid
Superseding:GB/T 14926.24-2001 Laboratory animal - Method for examination of pneumonia virus of mice (PVM)
Target Language: English
File Format: PDF
Word Count: 7500 words
Translation Price(USD): 225.0
Delivery: via email in 1~3 business day
GB/T 14926.24-2026 Laboratory animal—Method for examination of pneumonia virus of mice (PVM) English, Anglais, Englisch, Inglés, えいご This is a draft translation for reference among interesting stakeholders. The finalized translation (passing through draft translation, self-check, revision and verification) will be delivered upon being ordered. ICS 13.220.10 CCS H 57 National Standard of the People's Republic of China ‌GB/T 14926.24-2026 Replaces GB/T 14926.24-2001 Laboratory animal - Method for examination of pneumonia virus of mice (PVM) 实验动物 小鼠肺炎病毒检测方法 Issue date: 2026-01-28 Implementation date: 2027-02-01 Issued by the General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China the Standardization Administration of the People's Republic of China Contents Foreword Introduction 1 Scope 2 Normative References 3 Terms and Definitions 4 Principle 5 Reagents and Equipment 6 Detection Methods 7 Result Interpretation 8 Result Reporting Laboratory Animals — Detection Method for Pneumonia Virus of Mice 1 Scope This document describes detection methods for Pneumonia virus of mice (PVM). This document applies to the detection of PVM in mice, rats, hamsters, guinea pigs, as well as in experimental inocula and environmental samples from laboratory animal facilities. 2 Normative References The following documents are referred to in the text in such a way that some or all of their content constitutes requirements of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. GB/T 14926.42 Laboratory animal – Bacteriological examination – Collection of specimens GB/T 14926.50 Laboratory animal – Enzyme-linked immunosorbent assay GB/T 14926.51 Laboratory animal – Immunoenzyme assay GB/T 14926.52 Laboratory animal – Immunofluorescence assay 3 Terms and Definitions No terms and definitions are required for this document. 4 Principle 4.1 Principle of Antibody Detection Based on immunological principles, PVM antigen is used to detect PVM antibodies in the serum of mice, rats, hamsters, and guinea pigs. 4.2 Principle of Nucleic Acid Detection Based on molecular biology principles, the unique genomic nucleic acid sequences of Pneumonia virus of mice can be identified by nucleic acid amplification techniques such as polymerase chain reaction (PCR), thereby obtaining the target gene or fluorescent signal for detection. 5 Reagents and Equipment 5.1 Reagents 5.1.1 Enzyme-linked Immunosorbent Assay (ELISA) Antigen 5.1.1.1 Specific Antigen After infecting mice with PVM and awaiting the onset of disease, collect the lungs, grind them, and prepare a 10% suspension. Centrifuge at 3000 r/min for 10 min, and use the supernatant to infect BHK21 cells. Allow adsorption for 1.5 h to 2 h, add maintenance medium, and culture for 10 to 14 days. Harvest when cytopathic effect (CPE) reaches +++. Freeze-thaw 3 times or sonicate. Remove cell debris by low-speed centrifugation. Concentrate the supernatant by ultracentrifugation to prepare the ELISA antigen. 5.1.1.2 Normal Antigen Supernatant obtained by freeze-thawing and disrupting uninfected BHK21 cells, followed by low-speed centrifugation to remove cell debris. 5.1.2 Antigen Slides Infect BHK21 cells with PVM and culture for 5 to 7 days. When CPE reaches ++ to +++, disperse the cells with trypsin, wash with phosphate-buffered saline (PBS), and prepare smears. Air dry at room temperature. Fix with cold acetone for 10 minutes. Store at -20°C. 5.1.3 Positive Serum Antiserum obtained by immunizing specific pathogen free (SPF) mice, rats, guinea pigs, and hamsters with PVM. 5.1.4 Negative Serum Serum from SPF mice, rats, guinea pigs, and hamsters. 5.1.5 Enzyme Conjugate Horseradish peroxidase, etc. labeled goat or rabbit anti-mouse, rat, guinea pig, hamster IgG antibodies, used for detecting corresponding animal serum antibodies. Horseradish peroxidase-labeled Staphylococcal Protein A (SPA) can be used for detecting serum antibodies in mice, guinea pigs, and hamsters. 5.1.6 Fluorescent Conjugate Fluorescein isothiocyanate, etc. labeled goat or rabbit anti-mouse, rat, guinea pig, hamster IgG antibodies, used for detecting corresponding animal serum antibodies. 5.1.7 Primers and Probes Synthesize primers and probes according to the sequences in Table 1. Prepare primers and probes as 10 μmol/L stock solutions using RNase-free deionized water. Store at -20°C. 5.2 Equipment 5.2.1 Microplate reader. 5.2.2 Fluorescence microscope. 5.2.3 Ordinary light microscope. 5.2.4 37°C incubator or water bath. 5.2.5 Real-time quantitative PCR instrument. 6 Detection Methods 6.1 Collect serum according to GB/T 14926.42. 6.2 Collect organ tissues, cecal contents or feces, experimental inocula, and environmental samples from laboratory animal facilities according to Appendix A. 6.3 Use the ELISA method for serological detection, operating according to GB/T 14926.50. 6.4 Use the indirect immunofluorescence assay (IFA) method for serological detection, operating according to GB/T 14926.52. 6.5 Use the immunoenzyme assay (IEA) method for serological detection, operating according to GB/T 14926.51. 6.6 Use the real-time quantitative RT-PCR method for nucleic acid detection, operating according to Appendix A. 7 Result Interpretation 7.1 Serological Detection For positive results, retest using the same serological method or another serological method. If still positive, the result is interpreted as PVM antibody positive. 7.2 Nucleic Acid Detection For positive or suspicious results, retest using the same method. If still positive or suspicious, the result is interpreted as positive.
Code of China
Standard
GB/T 14926.24-2026  Laboratory animal—Method for examination of pneumonia virus of mice (PVM) (English Version)
Standard No.GB/T 14926.24-2026
Statusto be valid
LanguageEnglish
File FormatPDF
Word Count7500 words
Price(USD)225.0
Implemented on2026-5-1
Deliveryvia email in 1~3 business day
Detail of GB/T 14926.24-2026
Standard No.
GB/T 14926.24-2026
English Name
Laboratory animal—Method for examination of pneumonia virus of mice (PVM)
Chinese Name
实验动物 小鼠肺炎病毒检测方法
Chinese Classification
B44
Professional Classification
GB
ICS Classification
Issued by
SAMR, SAC
Issued on
2026-01-28
Implemented on
2026-5-1
Status
to be valid
Superseded by
Superseded on
Abolished on
Superseding
GB/T 14926.24-2001 Laboratory animal - Method for examination of pneumonia virus of mice (PVM)
Language
English
File Format
PDF
Word Count
7500 words
Price(USD)
225.0
Keywords
GB/T 14926.24-2026, GB 14926.24-2026, GBT 14926.24-2026, GB/T14926.24-2026, GB/T 14926.24, GB/T14926.24, GB14926.24-2026, GB 14926.24, GB14926.24, GBT14926.24-2026, GBT 14926.24, GBT14926.24
Introduction of GB/T 14926.24-2026
GB/T 14926.24-2026 Laboratory animal—Method for examination of pneumonia virus of mice (PVM) English, Anglais, Englisch, Inglés, えいご This is a draft translation for reference among interesting stakeholders. The finalized translation (passing through draft translation, self-check, revision and verification) will be delivered upon being ordered. ICS 13.220.10 CCS H 57 National Standard of the People's Republic of China ‌GB/T 14926.24-2026 Replaces GB/T 14926.24-2001 Laboratory animal - Method for examination of pneumonia virus of mice (PVM) 实验动物 小鼠肺炎病毒检测方法 Issue date: 2026-01-28 Implementation date: 2027-02-01 Issued by the General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China the Standardization Administration of the People's Republic of China Contents Foreword Introduction 1 Scope 2 Normative References 3 Terms and Definitions 4 Principle 5 Reagents and Equipment 6 Detection Methods 7 Result Interpretation 8 Result Reporting Laboratory Animals — Detection Method for Pneumonia Virus of Mice 1 Scope This document describes detection methods for Pneumonia virus of mice (PVM). This document applies to the detection of PVM in mice, rats, hamsters, guinea pigs, as well as in experimental inocula and environmental samples from laboratory animal facilities. 2 Normative References The following documents are referred to in the text in such a way that some or all of their content constitutes requirements of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. GB/T 14926.42 Laboratory animal – Bacteriological examination – Collection of specimens GB/T 14926.50 Laboratory animal – Enzyme-linked immunosorbent assay GB/T 14926.51 Laboratory animal – Immunoenzyme assay GB/T 14926.52 Laboratory animal – Immunofluorescence assay 3 Terms and Definitions No terms and definitions are required for this document. 4 Principle 4.1 Principle of Antibody Detection Based on immunological principles, PVM antigen is used to detect PVM antibodies in the serum of mice, rats, hamsters, and guinea pigs. 4.2 Principle of Nucleic Acid Detection Based on molecular biology principles, the unique genomic nucleic acid sequences of Pneumonia virus of mice can be identified by nucleic acid amplification techniques such as polymerase chain reaction (PCR), thereby obtaining the target gene or fluorescent signal for detection. 5 Reagents and Equipment 5.1 Reagents 5.1.1 Enzyme-linked Immunosorbent Assay (ELISA) Antigen 5.1.1.1 Specific Antigen After infecting mice with PVM and awaiting the onset of disease, collect the lungs, grind them, and prepare a 10% suspension. Centrifuge at 3000 r/min for 10 min, and use the supernatant to infect BHK21 cells. Allow adsorption for 1.5 h to 2 h, add maintenance medium, and culture for 10 to 14 days. Harvest when cytopathic effect (CPE) reaches +++. Freeze-thaw 3 times or sonicate. Remove cell debris by low-speed centrifugation. Concentrate the supernatant by ultracentrifugation to prepare the ELISA antigen. 5.1.1.2 Normal Antigen Supernatant obtained by freeze-thawing and disrupting uninfected BHK21 cells, followed by low-speed centrifugation to remove cell debris. 5.1.2 Antigen Slides Infect BHK21 cells with PVM and culture for 5 to 7 days. When CPE reaches ++ to +++, disperse the cells with trypsin, wash with phosphate-buffered saline (PBS), and prepare smears. Air dry at room temperature. Fix with cold acetone for 10 minutes. Store at -20°C. 5.1.3 Positive Serum Antiserum obtained by immunizing specific pathogen free (SPF) mice, rats, guinea pigs, and hamsters with PVM. 5.1.4 Negative Serum Serum from SPF mice, rats, guinea pigs, and hamsters. 5.1.5 Enzyme Conjugate Horseradish peroxidase, etc. labeled goat or rabbit anti-mouse, rat, guinea pig, hamster IgG antibodies, used for detecting corresponding animal serum antibodies. Horseradish peroxidase-labeled Staphylococcal Protein A (SPA) can be used for detecting serum antibodies in mice, guinea pigs, and hamsters. 5.1.6 Fluorescent Conjugate Fluorescein isothiocyanate, etc. labeled goat or rabbit anti-mouse, rat, guinea pig, hamster IgG antibodies, used for detecting corresponding animal serum antibodies. 5.1.7 Primers and Probes Synthesize primers and probes according to the sequences in Table 1. Prepare primers and probes as 10 μmol/L stock solutions using RNase-free deionized water. Store at -20°C. 5.2 Equipment 5.2.1 Microplate reader. 5.2.2 Fluorescence microscope. 5.2.3 Ordinary light microscope. 5.2.4 37°C incubator or water bath. 5.2.5 Real-time quantitative PCR instrument. 6 Detection Methods 6.1 Collect serum according to GB/T 14926.42. 6.2 Collect organ tissues, cecal contents or feces, experimental inocula, and environmental samples from laboratory animal facilities according to Appendix A. 6.3 Use the ELISA method for serological detection, operating according to GB/T 14926.50. 6.4 Use the indirect immunofluorescence assay (IFA) method for serological detection, operating according to GB/T 14926.52. 6.5 Use the immunoenzyme assay (IEA) method for serological detection, operating according to GB/T 14926.51. 6.6 Use the real-time quantitative RT-PCR method for nucleic acid detection, operating according to Appendix A. 7 Result Interpretation 7.1 Serological Detection For positive results, retest using the same serological method or another serological method. If still positive, the result is interpreted as PVM antibody positive. 7.2 Nucleic Acid Detection For positive or suspicious results, retest using the same method. If still positive or suspicious, the result is interpreted as positive.
Contents of GB/T 14926.24-2026
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