Title of article
Highly sensitive polymerase chain reaction-free quantum dot-based quantification of forensic genomic DNA Original Research Article
Author/Authors
Yu Kyung Tak، نويسنده , , Won-Young Kim، نويسنده , , Min Jung Kim، نويسنده , , Eunyoung Han، نويسنده , , Myun Soo Han، نويسنده , , Jong Jin Kim، نويسنده , , Wook Kim، نويسنده , , Jong-Eun Lee، نويسنده , , Joon Myong Song، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2012
Pages
7
From page
85
To page
91
Abstract
Forensic DNA samples can degrade easily due to exposure to light and moisture at the crime scene. In addition, the amount of DNA acquired at a criminal site is inherently limited. This limited amount of human DNA has to be quantified accurately after the process of DNA extraction. The accurately quantified extracted genomic DNA is then used as a DNA template in polymerase chain reaction (PCR) amplification for short tandem repeat (STR) human identification. Accordingly, highly sensitive and human-specific quantification of forensic DNA samples is an essential issue in forensic study. In this work, a quantum dot (Qdot)-labeled Alu sequence was developed as a probe to simultaneously satisfy both the high sensitivity and human genome selectivity for quantification of forensic DNA samples. This probe provided PCR-free determination of human genomic DNA and had a 2.5-femtogram detection limit due to the strong emission and photostability of the Qdot. The Qdot-labeled Alu sequence has been used successfully to assess 18 different forensic DNA samples for STR human identification.
Keywords
Forensic DNA samples , Alu sequence , STR human identification , Quantum dot
Journal title
Analytica Chimica Acta
Serial Year
2012
Journal title
Analytica Chimica Acta
Record number
1028222
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