SN/T 4603-2016 English PDFUS$229.00 ยท In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. SN/T 4603-2016: Detection of toxigenic gene of Vibrio parahaemolyticus in food and water for export - Multiplex PCR method and multiplex real-time PCR method Status: Valid
Basic dataStandard ID: SN/T 4603-2016 (SN/T4603-2016)Description (Translated English): Detection of toxigenic gene of Vibrio parahaemolyticus in food and water for export - Multiplex PCR method and multiplex real-time PCR method Sector / Industry: Commodity Inspection Standard (Recommended) Classification of Chinese Standard: X04 Word Count Estimation: 10,121 Date of Issue: 2016-08-23 Date of Implementation: 2017-03-01 Regulation (derived from): State-Quality-Inspection-Certification (2016)438 Issuing agency(ies): General Administration of Customs SN/T 4603-2016: Detection of toxigenic gene of Vibrio parahaemolyticus in food and water for export - Multiplex PCR method and multiplex real-time PCR method---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. Detection of toxigenic gene of Vibrio parahaemolyticus in food and water for export-Mutiplex PCR method and mutiplex real-time PCR method People's Republic of China Exit Inspection and Quarantine standards Export food and water producing Vibrio parahaemolyticus Common pathogenic gene detection methods multiplex PCR and Multiple real-time fluorescent PCR method 2016-08-23 released 2017-03-01 Implementation People's Republic of China General Administration of Quality Supervision, Inspection and Quarantine released ForewordThis standard was drafted in accordance with the rules given in GB/T 1.1-2009. The "United States FDA Bacteriology Analysis Manual," Chapter Vibrio.2004 (Chapter9.Vibrio2004ofFDABacteriological AnalyticalManual) and SN/T 2424-2010 "rapid detection of Vibrio parahaemolyticus in imported and exported food and real-time detection methods Light PCR method "primer sequences combined together to form a multiplex PCR system. This standard is proposed and managed by the National Certification and Accreditation Administration Committee. This standard was drafted by Yunnan Entry-Exit Inspection and Quarantine of People's Republic of China, Shanghai Entry-Exit Inspection and Quarantine of the People's Republic of China Bureau, Shanghai Jiaotong University, Shanghai Clinical Laboratory Center, Kunming Xishan District Center for Disease Control and Prevention. The main drafters of this standard. Chen Liping, Liu Zhongmin, Zhang Jilun, Chen Yun, Zhang Jianhua, Shi Xianming, Wang Dapeng, Wang Qingzhong, Wang Jue. Export food and water producing Vibrio parahaemolyticus Common pathogenic gene detection methods multiplex PCR and Multiple real-time fluorescent PCR method1 ScopeThis standard specifies the production of Vibrio parahaemolyticus multiplex PCR and multiple real-time fluorescent PCR detection method. This standard applies to seafood, seafood condiments, water production in the detection of Vibrio parahaemolyticus common pathogenic bacteria genes.2 Normative referencesThe following documents for the application of this document is essential. For dated references, only the dated version applies to this article Pieces. For undated references, the latest edition (including all amendments) applies to this document. National Food Safety Standard Microbiological Examination of Food Vibrio parahaemolyticus test GB/T 6682 analytical laboratory water specifications and test methods GB 19489 laboratory biosafety common requirements GB/T 27403 laboratory quality control specification food molecular biology test The United States FDA Bacteriology Analysis Manual ninth chapter Vibrio.2004 (Chapter9.Vibrio2004ofFDABacteriological AnalyticalManual)3 Terms and definitionsThe following terms and definitions apply to this document. 3.1 Multiplex PCR mutiplexPCR In the same reaction system by adding more than one pair of primers, while detecting several target gene PCR method. 3.2 Multiplex real-time PCR mutiplexreal-timePCR In the same reaction system by adding more than one pair of primers, simultaneous detection of several target genes by real-time fluorescence PCR method.4 AbbreviationsThe following abbreviations apply to this document. tdh. Heat-resistant hemolytic toxins corresponding gene (thermostabledirecthemolysin) tlh. Heat-labile hemolytic toxin corresponding gene (thermolabilehemolysin) trh. Heat-resistant direct hemolytic toxin-related hemolytic toxins corresponding gene (thermostablerelatedhemolysin) ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of SN/T 4603-2016_English be delivered?Answer: Upon your order, we will start to translate SN/T 4603-2016_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. The lengthier the document the longer the lead time.Question 2: Can I share the purchased PDF of SN/T 4603-2016_English with my colleagues?Answer: Yes. The purchased PDF of SN/T 4603-2016_English will be deemed to be sold to your employer/organization who actually pays for it, including your colleagues and your employer's intranet.Question 3: Does the price include tax/VAT?Answer: Yes. 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