GB/T 28229-2011 English PDFUS$259.00 · In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. GB/T 28229-2011: Detection of diarrheagenic Escherichia coli in ballast water of entry-exit ships Status: Valid
Basic dataStandard ID: GB/T 28229-2011 (GB/T28229-2011)Description (Translated English): Detection of diarrheagenic Escherichia coli in ballast water of entry-exit ships Sector / Industry: National Standard (Recommended) Classification of Chinese Standard: C51 Classification of International Standard: 07.100.20 Word Count Estimation: 11,146 Date of Issue: 2011-12-30 Date of Implementation: 2012-05-01 Regulation (derived from): Announcement of Newly Approved National Standards No. 23 of 2011 Issuing agency(ies): General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China Summary: This standard specifies the entry and exit of ships' ballast water and diarrhea Escherichia coli (diarrheagenic Escherichia coli) testing procedures and methods. This standard applies to the entry-exit ship ballast water diarrhea detection of Escherichia coli. GB/T 28229-2011: Detection of diarrheagenic Escherichia coli in ballast water of entry-exit ships---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 diarrheagenic Escherichia coli in ballast water of entry-exit ships ICS 07.100.20 C51 National Standards of People's Republic of China Entry and exit of ships ballast water cause diarrhea E. coli Testing method Issued on. 2011-12-30 2012-05-01 implementation Administration of Quality Supervision, Inspection and Quarantine of People's Republic of China Standardization Administration of China released ForewordThis standard was drafted in accordance with GB/T 1.1-2009 given rules. The revised standard used by the US Food and Drug Administration (FDA) "bacteriological test manual. diarrhea caused by Escherichia coli" (2009 July) (BAM. DiarrheagenicEscherichiacoli, July2009). The main difference between this standard and the FDA approach are. --- Deletion of some virulence factor detecting step; --- Delete real-time PCR screening step; --- Culture temperature from 35 ℃ ± 0.5 ℃ revised to 36 ℃ ± 1 ℃. This standard was proposed by the State Administration of Quality Supervision, Inspection and Quarantine. The standard by the China Academy of Inspection and Quarantine. This standard was drafted. China Inspection and Quarantine Science Research Institute, People's Republic of China Qinhuangdao Exit Inspection and Quarantine, the Chinese people Exit Inspection and Quarantine of the Republic of Guangzhou. The main drafters of this standard. Wang Lin, Zhang Shun, normally forest, Lijun Cheng, Zhang Yue, Li there, Li Xin, Nie Weizhong, Liao Ruyan, Chen Chuntian, Chi Ying, Liu Endong, Han Hui. Entry and exit of ships ballast water cause diarrhea E. coli Testing method1 ScopeThis standard specifies the entry and exit of ships ballast water cause diarrhea Escherichia coli (diarrheagenicEscherichiacoli) testing procedures And methods. This standard applies to the entry and exit of ships' ballast water cause diarrhea E. coli detected.2 DefinitionsThe following terms and definitions apply to this document. 2.1 Diarrhea caused by Escherichia coli diarrheagenicEscherichiacoli Part of the genus Escherichia virulent, can cause diarrhea, collectively known strains of human disease, generally including enteropathogenic Escherichia coli (EPEC), enterohemorrhagic Escherichia coli (EHEC), intestinal invasive Escherichia coli (EIEC ), enterotoxigenic large Escherichia coli (ETEC) and the like.3 equipment and materials3.1 Refrigerator. 2 ℃ ~ 8 ℃. 3.2 incubator. 36 ℃ ± 1 ℃, 44 ℃ ± 1 ℃. 3.3 filter collection device bacteria. 3.4 UV lamp. wavelength 365nm. 3.5 sterile conical flask. 500mL. 3.6 sterile pipette. 25mL, accurate to 0.1mL. 3.7 Pipette. 0.1mL, accurate to 0.01mL. 3.8 inoculating loop. 3.9 inoculating needle. 3.10 sterile Petri dish. 90mm. 4 media and reagents 1) 1) recommends using a commercial medium and biochemical reaction tube to ensure stable quality, biochemical reactions can also be used to identify microorganisms automatic biochemical equipment to complete. 4.1 brain heart infusion broth (BHI). 4.2 Double tryptone phosphate broth (dTP). See A.1. 4.3 EHEC enrichment broth (EEB). See A.2. 4.4 eosin methylene blue agar (EMB). See A.3. 4.5 MacConkey agar (MAC). see A.4. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of GB/T 28229-2011_English be delivered?Answer: Upon your order, we will start to translate GB/T 28229-2011_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 GB/T 28229-2011_English with my colleagues?Answer: Yes. The purchased PDF of GB/T 28229-2011_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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