Presley L A, Baumstark A L, Dixon A
DNA Analysis Unit, FBI Laboratory, Washington, D.C.
J Forensic Sci. 1993 Sep;38(5):1028-36.
The apparent stability of DNA in forensic samples has permitted the successful application of several techniques such as polymerase chain reaction (PCR)-based and restriction fragment length polymorphisms (RFLP) analysis to forensic cases. PCR-based typing of the HLA-DQ alpha region in forensic casework has been shown to be a valid and reliable technique. This inherent stability of DNA in forensic evidence has led us to address the question of whether DNA could successfully withstand certain evidence processes such as latent fingerprint and electrostatic detection apparatus (ESDA) processing and still yield a sufficient quantity and quality of DNA for PCR HLA DQ alpha typing. Through testing done with biological material on simulated and casework envelope, stamp, and cigarette butt type evidence, it was determined that samples could be processed for specific latent fingerprint and ESDA examinations and still yield sufficient DNA for conclusive HLA DQ alpha typing results.
法医样本中DNA的明显稳定性使得几种技术得以成功应用于法医案件,如基于聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)分析。基于PCR的法医案件中HLA - DQα区域分型已被证明是一种有效且可靠的技术。法医证据中DNA的这种固有稳定性促使我们探讨DNA是否能够成功经受某些证据处理过程,如潜在指纹和静电检测装置(ESDA)处理,并且仍能产生足够数量和质量的DNA用于PCR HLA DQα分型。通过对模拟和实际案件中的信封、邮票和烟头类型证据上的生物材料进行测试,确定样本可以进行特定的潜在指纹和ESDA检查,并且仍能产生足够的DNA以获得确凿的HLA DQα分型结果。