関連する実験動画

Updated: May 2, 2026

Fabrication and Implantation of Miniature Dual-element Strain Gages for Measuring In Vivo Gastrointestinal Contractions in Rodents.
09:29

Fabrication and Implantation of Miniature Dual-element Strain Gages for Measuring In Vivo Gastrointestinal Contractions in Rodents.

Published on: September 18, 2014

10.3K

上向きに変換するマイクロゲージは,in vivoの内光力動態を明らかにする

Jason R Casar1, Claire A McLellan2, Cindy Shi2

  • 1Department of Materials Science and Engineering, Stanford University, Stanford, CA, USA. jcasar@stanford.edu.

Nature
|January 1, 2025
PubMed
まとめ

研究者は体内の力を測定するために 摂取可能な光学マイクロゲージを開発しました これらのセンサーは,Caenorhabditis elegans丸虫の餌力を定量化し,10μNの噛み力を明らかにしました.

さらに関連する動画

Using a Microfluidics Device for Mechanical Stimulation and High Resolution Imaging of C. elegans10:39

Using a Microfluidics Device for Mechanical Stimulation and High Resolution Imaging of C. elegans

Published on: February 19, 2018

10.6K
In Vivo Luminal Measurement of Distension-Evoked Urothelial ATP Release in Rodents09:17

In Vivo Luminal Measurement of Distension-Evoked Urothelial ATP Release in Rodents

Published on: September 7, 2022

1.5K

関連する概念動画

Power Expended by a Constant Force00:57

Power Expended by a Constant Force

The relationship between work done and the time taken to do it can be explained using the concept of power. For example, several sprinters in a race may have the same velocity when they reach the finish line, therefore doing the same amount of work, but the winner does it in the least amount of time. Thus, power is defined as the rate of doing work. Since work can vary as a function of time, the average power is defined as the work done during a time interval, divided by the time interval.
7.8K
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...
1.9K