Abstract

Whole blood obtained by venipucture was collected in EDTA vacutainer tubes from unrelated individuals residing in Changsha, China. The DNA was extracted by phenol chloroform method (1). PCR amplification was performed using the AmpFlSTR Profiler Plus PCR amplification kit (PE-Biosystems, Foster City, CA) following the manufacturer's protocol (2). The amplified products were separated and detected using the ABI Prism 377 DNA sequencer (PE-Biosystems, Foster City, CA). The data were analyzed using The Promega Software, POWERSTATS.

Author Information

Ma, Y
National Laboratory of Medical Genetics, Central South University, Hunan, China
Gong, B
Forensic Science Research and Training Center, Intermediate People's Court of Changsha, Hunan, China
Xia, J
National Laboratory of Medical Genetics, Central South University, Hunan, China
Deng, H
National Laboratory of Medical Genetics, Central South University, Hunan, China
Pan, Q
National Laboratory of Medical Genetics, Central South University, Hunan, China
Li, Q
National Laboratory of Medical Genetics, Central South University, Hunan, China
Dai, H
National Laboratory of Medical Genetics, Central South University, Hunan, China
Wen, S
National Laboratory of Medical Genetics, Central South University, Hunan, China
Xia, K
National Laboratory of Medical Genetics, Central South University, Hunan, China
Pages: 2
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Stock #: JFS15269J
ISSN: 0022-1198
DOI: 10.1520/JFS15269J