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  • 09월 03일 23시 이후 : 초록수정 불가능, 일정확인 및 검색만 가능

제122회 대한화학회 학술발표회, 총회 및 기기전시회 안내 Highly sensitive molecular diagnostics using SERS-PCR

등록일
2018년 8월 23일 10시 38분 32초
접수번호
2515
발표코드
ANAL1.O-11 이곳을 클릭하시면 발표코드에 대한 설명을 보실 수 있습니다.
발표시간
목 10시 : 05분
발표형식
구두발표
발표분야
Analytical Chemistry - Oral Presentation of Young Analytical Chemists I
저자 및
공동저자
Yixuan Wu, Jaebum Choo1,*
Bionano Technology, Hanyang University, Korea
1Department of Bionano Engineering, Hanyang University, Korea
Recently, quantitative real-time PCR (QPCR) have been extensively used for the diagnosis of a wide range of infectious diseases. This technique found valuable clinical application in the diagnosis of viral diseases. However, QPCR suffers from several problems including time-consuming process and high fluorescent background signal. In the present work, we developed a novel molecular diagnostic method using SERS-PCR for the sensitive and specific detection of target genes. Due to the characteristics of amplifying Raman signals by factors up to 10-14 orders of magnitude and unique molecular fingerprinting information, surface-enhanced Raman scattering (SERS)-based biosensors provide ultrahigh sensitivity and have more advantages over the fluorescent detection method. In the present study, we employed an asymmetric-PCR to amplify the target gene in a short time, and then a SERS detection technique has been used for its highly sensitive detection. By combining the PCR and SERS as a detection tool, it would prove to be effective for the rapid and sensitive detection of a low concentration of target. References 1. Kneipp, K., Wang, Y., Kneipp, H., Perelman, L. T., & Itzkan, I, Phys. Rev. Lett. 78, 1667 (1997). 2. Wu, Y., Jiang, T., Wu, Z., & Yu, R, Biosens. Bioelectron, 99, 646-652 (2018). Keywords: SERS-PCR, Pseudomonas aeruginosa, Ratiometirc gene detection, molecular diagnostics

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