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PCR Amplification of DNA Extracted from Paraffin-Embedded Tissue

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dc.contributor.authorLee, Jung Bin-
dc.contributor.authorLee, Yoon Seong-
dc.date.accessioned2009-08-06T23:59:01Z-
dc.date.available2009-08-06T23:59:01Z-
dc.date.issued1992-06-
dc.identifier.citationSeoul J Med, Vol.33 No.2, pp. 121-125-
dc.identifier.issn0582-6802-
dc.identifier.urihttps://hdl.handle.net/10371/6347-
dc.description.abstractThe polymerase chain reaction(PCR) DNA amplification method is a
powerful new tool in the field of individual identification or examination of medicolegal
evidences. Usually DNA is extracted from fresh tissue, blood, semen or dried specimen.
We try to find suitable way to obtain DNA from paraffin-embedded tissue(PET), the
most common preparation in pathological archives. Since PET processing conditions
vary in their suitability for amplification, variable methods l)simple long incubation 2)
xylene method 3)heating method 4)ether method were tried. Two VNTR loci of 017530
and apolipoprotein B gene were used for PCR amplification. The deparaffination process
using ether shows the best result in the DNA extraction and PCR amplication.
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dc.language.isoen-
dc.publisherSeoul National University College of Medicine-
dc.subjectPCR-
dc.subjectParaffin-embedded tissue(PET)-
dc.subjectEther-
dc.titlePCR Amplification of DNA Extracted from Paraffin-Embedded Tissue-
dc.typeSNU Journal-
dc.contributor.AlternativeAuthor이정빈-
dc.contributor.AlternativeAuthor이윤성-
dc.citation.journaltitle서울 의대 잡지-
dc.citation.journaltitle서울 의대 학술지-
dc.citation.journaltitleSeoul Journal of Medicine-
dc.citation.endpage125-
dc.citation.number2-
dc.citation.pages121-125-
dc.citation.startpage121-
dc.citation.volume33-
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