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dc.contributor.authorRosy Hutami
dc.contributor.authorJoko Hermanianto
dc.contributor.authorNancy Dewi Yuliana
dc.date.accessioned2014-06-04T07:45:53Z
dc.date.available2014-06-04T07:45:53Z
dc.date.issued2014-02
dc.identifier.issn2355-4029
dc.identifier.urihttp://repository.ipb.ac.id/handle/123456789/69054
dc.description.abstractcommercially available conventional PCR, based on a multi-copy target cytochrome b (cyt b) using porcine specific primers, has been validated for the Halal/Kosher authentication of porcine detection. Detection of porcine DNA residue on najis affected equipments after ritual purification (sertu) is requred to provide initial data of syariah purification implementation in industrial equipments. In this study, the probability of conventional PCR method in observing porcine DNA residue on affected equipments after ritual purificated was 1:3. It means 75% of the sample analysis was disobservable using coventional PCR analysis method. The porcine DNA band was once found at 398 bp. The concentration of DNA extraction on the affected equipments varied from 2.4-24.2 ng/μl. The method were used Phire Direct PCR Dillution Buffer combining with Phusion High-Fidelity PCR kit.en
dc.language.isoid
dc.publisherProceeding of The 1st International Conference on Halal-Thoyib Industry & Research "Halal Industry and its Challenge Toward Global Safety and Prosperity". 19-20 Februari 2014. Halal-Thoyib Science Center. Brawijaya University
dc.titleDetection of Porcine DNA Residu By Polymerase Chain Reaction on Food Processing Equipments after Ritual Purificationen
dc.typeArticleen
dc.subject.keywordporcineen
dc.subject.keywordPCRen
dc.subject.keywordDNAen


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