Subin Kim, Myeonggwan Kim, Heeung Choi, Sujin Heo, Jaewon Lim
언어
영어(ENG)
URL
https://www.earticle.net/Article/A467639
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초록
영어
Biological evidence collected at crime scenes plays a crucial role in confirming the identities of individuals. Blood, particularly is a commonly encountered bodily fluid at such scenes, and fluids containing blood, such as saliva, semen, vaginal fluid, and urine, are excellent tools for personal identification. The accurate identification and collection of blood is essential for reconstructing crime scenes and subsequently identifying suspects. Blood is commonly found at crime scenes distributed across various surfaces and objects, serving as important evidence. The analysis of bloodstains provides valuable information about the events that occurred during a crime, and bloodstain analysis is a vital tool for reconstructing events at a crime scene. Initially, the presence of blood is confirmed based on factors such as time, conditions, and environment. Invisible bloodstains are identified by visually inspecting suspicious areas, followed by performing serological preliminary and confirmatory tests to determine the presence of blood. Notably, luminol and KM reagents are commonly used reagents at crime scenes. In cases where bloodstain analysis indicates a positive result, personal identification is conducted using nucleic acid (DNA) alongside confirmatory tests. Experimental results show that the luminol reagent exhibits higher sensitivity than the KM reagent. During DNA amplification, it is observed that factors such as time, conditions, and environment influence DNA amplification more than reagents. Furthermore, the STR marker D1S80 showed a more significant reduction compared to the TH01 marker. This experiment holds potential applicability in various crime scenes, offering foundational data regarding results based on sample types, temperature, environment, and time.
목차
Abstract Ⅰ. Introduction Ⅱ. Material and method 1. Materials and Equipment 2. Experimental Methods Ⅲ. Results 1. Preliminary Results from Skin and Fabric Samples 2. Quantification of DNA Extracted from Skin and Fabric Bloodstains 3. Analysis of DNA Extracted from Skin and Fabric Bloodstains Using Real-time PCR Ⅳ. Discussion Ⅴ. Conclusion Ⅵ. Acknowledgments Ⅶ. References
키워드
DNAEvidenceSkinFabricLuminolKM
저자
Subin Kim [ Department of Forensic Sciences, Graduate school, Catholic University of Pusan, Busan, Republic of Korea ]
Myeonggwan Kim [ Department of Forensic Sciences, Graduate school, Catholic University of Pusan, Busan, Republic of Korea/Next-Generation Industrial Field-Based Specialist Program for Molecular Diagnostics, Brain Busan 21 Plus Project, Graduate School, Catholic University of Pusan, Busan, Republic of Korea ]
Heeung Choi [ Department of Forensic Sciences, Graduate school, Catholic University of Pusan, Busan, Republic of Korea ]
Sujin Heo [ Department of Forensic Sciences, Graduate school, Catholic University of Pusan, Busan, Republic of Korea ]
Jaewon Lim [ Department of Forensic Sciences, Graduate school, Catholic University of Pusan, Busan, Republic of Korea/Department of Clinical Laboratory Sciences, College of Health Science, Catholic University of Pusan, Busan, Republic of Korea/ Next-Generation Industrial Field-Based Specialist Program for Molecular Diagnostics, Brain Busan 21 Plus Project, Graduate School, Catholic University of Pusan, Busan, Republic of Korea ]
Corresponding Author
법과학 분야는 사회정의 구현에 있어 크나큰 가치가 있음에도 불구하고 우리나라에서는 이 분야에 대한 인식이 미흡하여 선진 외국에 비해 침체되어 있는 실정이다. 이에 우리나라에서도 법과학 분야와 관련 있는 학계, 연구기관, 수사기관 등 유관 단체들로 구성된 한국 법과학회를 창립하여 이 분야를 활성화 시켜 과학수사를 한층 더 발전시키기 위함을 목적으로 한다.