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主营:化学试剂,CCK-8试剂盒,细胞检测,自噬研究,化学标记,生化试剂等
℡ 4000-520-616
℡ 4000-520-616
Dojindo/Microbial Viability Assay Kit-WST/500/M439
产品编号:M439
市  场 价:¥4860.00
场      地:美国(厂家直采)
产品分类: 蛋白类>多肽>多肽合成>
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:$243.00
品      牌: Dojindo
公司分类:
Dojindo/Microbial Viability Assay Kit-WST/500/M439
商品介绍
DescriptionApplicationReferencesDataManualS.D.S
Product DescriptionViable bacterial cell detections are very important for analyzing bacteria contamination in food or evaluating the cleanliness of facilities in order to protect us from food poisoning and infections. Bacterial cell detections are also used for the screening of sanitizing agents and drug resistance detections. Generally, counting the number of colonies on an agar plate is the standard method for determining the number of viable bacterial cells in samples. However, colony formations require one to several days. Dojindo’s Microbial Viability Assay Kit-WST can be used to determine the number of viable bacterial cells in a sample by a colorimetric method and can be applied to 96-well microplate assays. The electron mediator in the kit receives electrons from viable bacterial cells and transfers the electrones to WST, one of the water-soluble tetrazolium salts developed by Dojindo. Bacterial cell viability then can be determined by monitoring the color intensity of WST formazan dye. Since several types of media used for bacterial cell cultures and components do not interfere with the assay(Fig. 5), simply add the assay solution and incubate for one to several hours to determine the initial number of viable bacterial cells in the sample(Fig. 2). This assay kit was co-developed with the Biotechnology and Food Research Institute, Fukuoka Industrial Technology Center.

Fig. 1 Bacterial cell viability detection mechanism.

Assay DataFig. 2 Correlation between initial number of E. coli and time-dependent O.D. increase. The initial number of viable E.coli were determined by a colony counting method.

Fig. 3 Correlation between the initial number of SA and time-dependent O.D. increase. The initial number of viable SA were determined by the colony counting method.

Comparison Chart

Fig. 4 Influence of culture media or substances used for bacterial cell culture.The data indicated that WST is less sensitive to various culture media or substances which are used for bacterial cell culture. WST is a better tetrazolium salt than XTT for bacterial cell viability assays.

General Procedure 2Determination of the susceptibility of Staphylococcus aureus to oxacillinOxacillin: antimicrobial agent: 0-64 μg/mlMicroorganism: Staphylococcus aureus (SA)Methicillin-resistant Staphylococcus aureus (MRSA)1. Culture SA or MRSA with Mueller-Hintonmedium containing various concentrations of Oxacillin for 6 hours at 35ºC.2. Add Microbial Viability Assay solution equal to 1/20 the volume of the culture medium.3. Incubate for 2 hours at 35ºC.4. Measure the O.D. at 450 nm to determine the MIC (Minimum inhibitory concentration).

Fig. 4 Susceptibility test of SA and MRSA against Oxacillin*.The data indicated that MRSA has lower susceptibility than SA. The MICs of MRSA (32 μg/ml) and SA (0.5 μg/ml) are close to the MICs determined by the CLSI (Clinical and Laboratory Standards Institute) method.

1. T. Tsukatani, et al., Colorimetric cell proliferation assay for microorganisms in microtiter plate using water-soluble tetrazolium salts. J Microbiol Methods. 2008;75:109-116.2. T. Tsukatani, et al., Colorimetric microbial viability assay based on reduction of water-soluble tetrazolium salts for antimicrobial susceptibility testing and screening of antimicrobial substances. Anal Biochem. 2009;393:117-125.3. T. Tsukatani, et al., Determination of water-soluble vitamins using a colorimetric microbial viability assay based on the reduction of water-soluble tetrazolium salts. Food Chem.2011;127:711-7154. T. Tsukatani, et al., Comparison of the WST-8 colorimetric method and the CLSI broth microdilution method for susceptibility testing against drug-resistant bacteria. J Microbiol Methods. 2012;90:160-1665. Jeffrey C. Pommerville. 2014. Fundamentals of Microbiology: Body Systems Edition (3rd Third Edition), p.339. Burlington, MA: Jones & Bartlett Learning.

Appropriate Cell DensityTable 6 Initial cell number can reach O.D. 0.5 with 1-hour and 4-hour incubation.The initial cell number of each microorganism was determined by colony counting. Each microorganism cell culture was diluted with medium and 190 μl of the cell culture was added to each well. Then 10 μl of assay solution was added. The cells were incubated at 30oC or 37oC for 1 hour and 4 hours to determine how many cells are required to reach O.D.=0.5 at 460 nm.

Related Categories Microbial Viability Assay

品牌介绍

Dojindo Molecular Technologies,Inc.是美国领先的生命科学研究专用试剂盒和化学品分销商。我们通过提供优质的支持和创新产品,不断扩大客户的满意度,以扩大生命科学研究和开发领域。

我们的公司文化反映出“ Jin”(仁)字符背后的含义,即尊重和关爱他人。当我们公司执行上述任务时,“ Jin”精神始终处于我们思想的最前沿。  


我们如何开始

1996年

作为日本Dojindo实验室的子公司,Dojindo Molecular Technologies,Inc.在马里兰州盖瑟斯堡开业,这是新产品开发的主要设施。开发了诸如DNA损伤定量试剂盒SOD检测试剂盒WST标记试剂盒系列之类的产品,为全球客户提供现成的检测试剂盒。


2000

Dojindo Molecular Technologies,Inc.成为了另一个销售地点,将Dojindo产品带到了北美地区的研究专业人员手中。


2008年

我们搬迁至马里兰州罗克维尔,仅专注于北美的销售和营销活动。我们目前的位置非常接近美国国立卫生研究院(NIH),美国国家癌症研究所(NCI),FDA,约翰·霍普金斯大学的研究人员。


我们不仅向周边地区,而且向我们在美国,加拿大和南美的客户提供日本优质的客户支持和创新产品。

关于同人堂实验室

Dojindo Laboratories由螯合化学领域的著名研究人员上野敬平教授创立。同人堂实验室是1951年第一家将EDTA(乙二胺四乙酸)商业化的日本公司。自那以后,同人堂实验室一直在生产用于支持科学研究进展的试剂。Dojindo实验室的任务是开发用于生命科学研究的创新工具。Dojindo实验室致力于通过科学发现和开发新药物为改善生活质量做出贡献。


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