Session Details
[1BT-06]Dynamics analysis of lipids, proteins, and proteome by in situ chemical labeling
Wed. Nov 27, 2024 11:45 AM - 12:35 PM JST
Wed. Nov 27, 2024 2:45 AM - 3:35 AM UTC
Wed. Nov 27, 2024 2:45 AM - 3:35 AM UTC
Room 6(Fukuoka International Congress Center, 4F 411+412)
Chairman:Akira Sato(Carl Zeiss Co., Ltd.)
Chemical modification of biomolecules by synthetic probes is a powerful technique for creating useful molecular tools for biological research. For example, the selective attachment of fluorescent dyes to target proteins in cells or living animals allows various applications such as bioimaging, interaction detection, and activity regulation of proteins. In addition, direct functionalization of metabolites not directly encoded by genes, such as lipids, with synthetic probes enables dynamic analysis that cannot be achieved by conventional molecular biology-based techniques and genetic engineering. In this talk, I will introduce our recent works on in situ modification for biomolecules imaging with Zeiss microscopy and their applications in proteomics and genomics.
[1BT-06-01]Dynamics analysis of lipids, proteins, and proteome by in situ chemical labeling
〇Tomonori Tamura1 (1.Graduate School of Engineering, Kyoto University)
[1BT-06-02]Airyscan, vs. Lattice SIM, which would you choose?Introducing ZEISS multimodal super-resolution microscopy technology
〇Yasuhiko Sato1 (1.Light Microscopy Specialist, RMS, Carl Zeiss Co., Ltd.)