相关实验视频

Updated: Jul 23, 2025

An Optimized Single-Molecule Pull-Down Assay for Quantification of Protein Phosphorylation
07:45

An Optimized Single-Molecule Pull-Down Assay for Quantification of Protein Phosphorylation

Published on: June 6, 2022

3.0K

在现场解密等离子体纳米粒子大小受控酸化表皮生长因子受体在活细胞中

Hongyan Wang1, Yan Ding1, Yu Zhang2

  • 1First Affiliated Hospital of Anhui Medical University, Hefei 230000, China.

Chemical communications (Cambridge, England)
|July 13, 2023
PubMed
概括

金纳米颗粒 (GNP) 的大小影响表皮生长因子受体 (EGFR) 酸化. 这影响了使用暗场显微镜 (DFM) 观察到的EGFR向纳米探针的聚合.

更多相关视频

Studying the Stoichiometry of Epidermal Growth Factor Receptor in Intact Cells using Correlative Microscopy09:16

Studying the Stoichiometry of Epidermal Growth Factor Receptor in Intact Cells using Correlative Microscopy

Published on: September 11, 2015

8.4K
A Functional Assay for Gap Junctional Examination; Electroporation of Adherent Cells on Indium-Tin Oxide11:02

A Functional Assay for Gap Junctional Examination; Electroporation of Adherent Cells on Indium-Tin Oxide

Published on: October 18, 2014

10.0K

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...
2.2K