SN/T 3327-2012 English PDFUS$209.00 · In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. SN/T 3327-2012: Quarantine protocal for classic swine fever virus by loop-mediated isothermal amplification Status: Valid
Basic dataStandard ID: SN/T 3327-2012 (SN/T3327-2012)Description (Translated English): Quarantine protocal for classic swine fever virus by loop-mediated isothermal amplification Sector / Industry: Commodity Inspection Standard (Recommended) Word Count Estimation: 8,839 Quoted Standard: GB/T 18088; GB 19489-2008 Regulation (derived from): National Quality Inspection (2012) 777; industry standard filing Notice 2013 No. 4 (No. 160 overall) Issuing agency(ies): General Administration of Customs Summary: This standard specifies the method of operation of classical swine fever virus reverse transcriptase loop-mediated isothermal nucleic acid amplification testing. This standard applies to rapid screening of classical swine fever virus. SN/T 3327-2012: Quarantine protocal for classic swine fever virus by loop-mediated isothermal amplification---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 protocal for classic swine fever virus by loop-mediated isothermal amplification People's Republic of China Entry-Exit Inspection and Quarantine Standards Classical swine fever virus by reverse transcription loop-mediated isothermal Nucleic acid amplification tests Quarantineprotocalforclassicswinefevervirusbyloop-I mediated Issued on. 2012-12-12 2013-07-01 implementation People's Republic of China The State Administration of Quality Supervision, Inspection and Quarantine released ForewordThis standard was drafted in accordance with GB/T 1.1-2009 given rules. This standard is proposed and managed by the National Certification and Accreditation Administration Committee. This standard was drafted. People's Republic of China Shanghai Entry-Exit Inspection and Quarantine Bureau. The main drafters of this standard. Li Jian, Xiong Wei, Zhang Qiang, Jiang Jing, Qiu Lu, Wang Qiao whole, Huang Zhongrong, Hu Yongqiang. Classical swine fever virus by reverse transcription loop-mediated isothermal Nucleic acid amplification tests1 ScopeThis standard specifies the method of operation of classical swine fever virus by reverse transcription loop-mediated isothermal nucleic acid amplification detection. This standard applies to rapid screening of classical swine fever virus.2 Normative referencesThe following documents for the application of this document is essential. For dated references, only the dated version suitable for use herein Member. For undated references, the latest edition (including any amendments) applies to this document. GB/T 18088 Entry and Exit Animal Quarantine sampling GB 19489-2008 General requirements for laboratory biosafety3 OverviewClassical swine fever (classicalswinefever, CSF), is a kind of emergency by the classical swine fever virus (classicalswinefevervirus, CSFV) caused Resistance, heat resistance, highly contagious disease of swine breeding industry very serious harm. CSFV genotype positive strand RNA, genome about 123kb, contains only one large open reading frame (ORF). The standard use of loop-mediated isothermal nucleic acid amplification at a constant temperature Fast, efficient and specifically amplify located fever virus 5 'untranslated region (5'-UTR) of the target sequence, so as to achieve rapid detection purposes.4 Reagents and materials4.1 BstDNA polymerase (large fragment). enzyme concentration was 8U/μL, -20 ℃, avoid repeated freezing and thawing. 4.2 10 times ThermoPol polymerase buffer concentrate. -20 ℃ to save. 4.3 magnesium sulfate (MgSO4). concentration of 25mmol/L, -20 ℃ preservation. 4.4 AMV reverse transcriptase. reverse transcriptase concentration of 5U/μL, -20 ℃, avoid repeated freezing and thawing. 4.5 betaine solution (Betaine). concentration 5mol/L, -20 ℃, avoid repeated freezing and thawing. 4.6 dNTPs. containing dATP, dGTP, dCTP, dTTP each 10mmol/L, -20 ℃ preservation. 4.7 LAMP primer. primer dubbed the concentration of 25μmol/L, -20 ℃ stored for use. Its sequence is as follows. --- Being outwardly primer (CSFV-F3). 5'-AGC-TCC-CTG-GGT-GGT-CTA-3 '; --- Reverse outer primer (CSFV-B3). 5'-CCT-AAT-AGT-GGG-CCT-CTG-CA-3 '; --- Within the forward primer (CSFV-FIP). 5'-GCC-CTC-GTC-CAC-ATA-GCA-TCT-CAG-TAC-AGG-ACA- GTC-GTC-AGT-3 '; --- Within the reverse primer (CSFV-BIP). 5'-GCC-CAA-GAC-ACA-CCT-TAA-CCC-TTC-AGG-TCG-TAC- TCC-CAT-CAC-3 '; --- Forward loop primer (CSFV-LF). 5'-GGG-CTT-CTG-CTC-ACG-TCG-3 '; --- Reverse loop primer (CSFV-LB). 5'-GGT-CGC-TAG-GGT-GAA-ATC-3 '. 4.8 SYBRGreenⅠ fluorescent dye solution. -20 ℃ to save. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of SN/T 3327-2012_English be delivered?Answer: Upon your order, we will start to translate SN/T 3327-2012_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. 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