相关实验视频

Updated: Jun 6, 2026

Visualizing the Live Drosophila Glial-neuromuscular Junction with Fluorescent Dyes
10:53

Visualizing the Live Drosophila Glial-neuromuscular Junction with Fluorescent Dyes

Published on: May 13, 2009

10.9K

照亮D1 -Like受体:基于光的工具箱用于可视化D1和D5受体

Niklas Rosier1, Denise Mönnich1, Martin Nagl1

  • 1Institute of Pharmacy, University of Regensburg, Universitätsstraße 31, 93053, Regensburg, Germany.

Chembiochem : a European journal of chemical biology
|November 20, 2023
PubMed
概括

研究人员开发了一种新的光配体UR-NR435,用于可视化多巴胺D1类受体. 这种高亲和度,选择性中性抗剂是使用光显微镜研究神经系统疾病的理想选择.

关键词:
类似D1的受体.同焦点显微镜的共焦显微镜.多巴胺受体的多巴胺受体光联结体是一种光联结体.分子亮度 分子亮度

更多相关视频

Characterization of G Protein-coupled Receptors by a Fluorescence-based Calcium Mobilization Assay11:49

Characterization of G Protein-coupled Receptors by a Fluorescence-based Calcium Mobilization Assay

Published on: July 28, 2014

40.2K
High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy15:13

High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy

Published on: July 25, 2014

11.5K

相关概念视频

Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...