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peR Amplification of DNA Extracted from Formalin-Fixed Tissue

DC Field Value Language
dc.contributor.authorLee, Jung Bin-
dc.contributor.authorLee, Yoon Seong-
dc.date.accessioned2009-08-06T23:59:21Z-
dc.date.available2009-08-06T23:59:21Z-
dc.date.issued1992-06-
dc.identifier.citationSeoul J Med, Vol.33 No.1, pp. 115-119-
dc.identifier.issn0582-6802-
dc.identifier.urihttps://hdl.handle.net/10371/6349-
dc.description.abstractIn this study we try to confirm whether the DNA from formalin-fixed tissue
be suitable for forensic application such as individual identification or examination
of medicolegal evidences using PCR. Fresh placenta were taken from 18 different
women and DNA was extracted . Some portion of placenta were fixed in 10% buffered
neutral formalin for 24 hour and DNA was extracted. Two loci of DlS80 and D17S30
were used for PCR amplification. The amplification pattern were identical between fresh
tissue and formalin fixed tissue suggesting that the formalin fixed tissue can be used for
medicolegal situation. But the DNA from formalin seemed to be degraded as the fixation
time prolonged.
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dc.language.isoen-
dc.publisherSeoul National University College of Medicine-
dc.subjectFormalin-fixed tissue-
dc.subjectPCR-
dc.titlepeR Amplification of DNA Extracted from Formalin-Fixed 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.endpage119-
dc.citation.number1-
dc.citation.pages115-119-
dc.citation.startpage115-
dc.citation.volume33-
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