In experiment "Analysis of cell death in U2Os cells (live)", multiwell chambers of U2Os were observed using a Nikon Ti inverted epifluorescent microscope. Specific dyes were TMRM; nucview488. The re
Imaging mode: Gray Scale Visualization methods: Captured on a microscope using a Canon Rebel Ti5/6 or a one of the following eyepiece cameras: Swiftcam 3 Megapixel, OMAX 9.0 MP, AmScope MU300
Optical section series through adjacent protoplasmic astrocytes in rat hippocampal area CA1 intracellulaly injected Lucifer Yellow (green) and Alexa 568 (red) respectively, imaged with confocal micros
• This is a gliding motility assay using kinesin-1 and rhodamine labeled microtubules. • The buffer used was PEM (also known as BRB80) with the inclusion of 5528mM D2O. • Images were taken with an And
