Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/52270
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dc.contributor.authorMaslin Osathanunkulen_US
dc.contributor.authorKittisak Buddhachaten_US
dc.contributor.authorSiriwadee Chomdejen_US
dc.date.accessioned2018-09-04T09:22:55Z-
dc.date.available2018-09-04T09:22:55Z-
dc.date.issued2013-02-15en_US
dc.identifier.issn10960309en_US
dc.identifier.issn00032697en_US
dc.identifier.other2-s2.0-84870695160en_US
dc.identifier.other10.1016/j.ab.2012.09.036en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84870695160&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52270-
dc.description.abstractCoomassie brilliant blue (CBB) heated by microwave was used as a staining dye for measuring gelatinolytic activity. The quantity of gelatin remaining after incubation with bacterial collagenase was determined using the heated CBB, resulting in visible blue pellets. Dimethyl sulfoxide was added to dissolve the dye and measurement of the absorbance at 600 nm was done to detect the level of gelatin (up to 10 μg), with the limit of detection for the amount of collagenase at 50 ng. This approach is rapid, simple, and economic for the purpose of screening for pharmaceutical agents that possess inhibitory activity on collagenase. © 2012 Elsevier Inc. All rights reserved.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleA modified colorimetric method of gelatinolytic assay using bacterial collagenase type II as a modelen_US
dc.typeJournalen_US
article.title.sourcetitleAnalytical Biochemistryen_US
article.volume433en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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