Abstract

Bloodstains of 200 unrelated Han population individuals living in southern China, 100 unrelated Zhuang population individuals from Guangxi were prepared on sterilized filter and subsequently air dried. DNA was obtained from bloodstain specimens using Chelex 100 (3). PCR amplification was performed using primers labeled with fluorescent dye (2,3). The amplified products were separated and detected using ABI Prism 310 sequencer (PEBiosystems, Foster City, CA). The data were analyzed as published previously (4-6).

Author Information

Zheng, X
Institute of Forensic Science, Beijing, P. R. China
Ling, F
Beijing In-Exit Quarantine Bureau, Beijing, P. R. China
Dong, C
University of Haidian, Beijing, P. R. China
Dong, C
University of Haidian, Beijing, P. R. China
Shaojian Zhu, S
Institute of Forensic Science, Beijing, P. R. China
Kobilinsky, L
Li, J
Institute of Forensic Science, Beijing, P. R. China
Li, C
Institute of Forensic Science, Beijing, P. R. China
Pages: 2
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Stock #: JFS2003057
ISSN: 0022-1198
DOI: 10.1520/JFS2003057