GB/T 28228-2011 English PDFUS$229.00 · In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. GB/T 28228-2011: Detection of Listeria monocytogenes in ballast water of entry-exit ships Status: Valid
Basic dataStandard ID: GB/T 28228-2011 (GB/T28228-2011)Description (Translated English): Detection of Listeria monocytogenes 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: 10,157 Date of Issue: 2011-12-30 Date of Implementation: 2012-05-01 Adopted Standard: FDA BAM-2003, MOD 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 Listeria monocytogenes bacteria (Listeria monocytogenes) testing procedures and methods. This standard applies to the entry and exit of Ships' Ballast Water Listeria monocytogenes bacteria testing. GB/T 28228-2011: Detection of Listeria monocytogenes 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 Listeria monocytogenes 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 monocytes Test method of Listeria 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. Listeria monocytogenes bacteria in check Measure and count "(January 2003) (BAM. DetectionandenumerationofListeriamonocytogenes, January2003). The main difference between this standard and the FDA approach are. --- Increased screening step; --- Clear the counting step; --- Incubator temperature from 35 ℃ 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 Republic SZCIQ. The main drafters of this standard. Shun together, Wang Lin, Pangqiu Yan, Zhang Yue, Li has, Lijun Cheng, Li Xin, Nie Weizhong, Chen Chuntian, FORCES, Chi Ying, Zhao Bin, Han Hui. Entry and exit of ships ballast water monocytes Test method of Listeria1 ScopeThis standard specifies the entry and exit of ships' ballast water monocytogenes Listeria (Listeriamonocytogenes) detection process Order and method. This standard applies to detect the entry and exit of ships ballast water Listeria monocytogenes bacteria.2 Equipment and Materials2.1 Refrigerator. 2 ℃ ~ 8 ℃. 2.2 incubator. 30 ℃ ± 1 ℃, 36 ℃ ± 1 ℃. 2.3 Microscope. 10 × ~ 100 ×. 2.4 Sterile pipette or a sterile graduated cylinder. 1mL, 25mL, accurate to 0.1mL. 2.5 conical flask. 500mL. 2.6 sterile Petri dish. diameter of 90mm. 2.7 sterile tube. 16mm × 125mm. 2.8 inoculating loop. 2.9 inoculating needle. 2.10 Staphylococcus aureus (ATCC25923). 2.11 Rhodococcus equi (Rhodococcusequi). 2.12 Iraq's Listeria. 2.13 monocytogenes Listeria. Listeria innocua 2.14.3 media and reagents3.1 Listeria enrichment broth buffer (BLEB). See A.1. 3.2 PALCAM Agar. see A.2. 3.3 ALOA chromogenic medium 1). 3.4 containing 0.6% yeast extract of trypticase soy agar (TSAye). See A.3. 3.5 SIM medium power. see A.4. 3.6 5% sheep blood agar. see A.5. 3.7 Gram staining solution. 3.8 3% hydrogen peroxide solution. Test for catalase. 3.9 biochemical reaction tube 2). rhamnose, xylose, glucose, maltose, mannitol, MR/VP test. 1) provided by the French company AES product trade name, this information is given for convenience only user of this standard does not imply endorsement of the product, such as Other fruit products have the same effect, you can use these equivalent products. 2) recommend the use of commercially available biochemical reaction tube to ensure stable quality, can also be used biochemical automated microbial identification system completed. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of GB/T 28228-2011_English be delivered?Answer: Upon your order, we will start to translate GB/T 28228-2011_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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