WebMar 3, 2024 · The CYTO-ID dye is known to stain autophagic vesicles ( 24 ), and we have previously demonstrated similar results obtained by analyses of CYTO-ID staining and by detection of LC3-II ( 8 ). Forskolin enhanced the IR-induced autophagy, as revealed both by CYTO-ID staining and LC3-II detection ( Fig. 1A – D ).
Dynamin-2 deficiency causes age- and sex-dependent …
WebNov 2, 2024 · 2.12 Cyto-ID staining. Cells were treated with SCA (0, 4, 8, and 16 μmol/L) in 6-well plates for 24 h and then stained with Cyto-ID (37°C, 30 min; Enzo, New York, NY, United States). Excess dye was removed and the cells were stained with DAPI for 15 min and imaged using a live cell workstation (ZEISS). The above experiments were … WebMar 26, 2024 · Removing excessive platelets using acoustofluidic methods receives extensive attention due to their high efficiency and high yield. While the damage to the remaining cells, such as erythrocytes and leukocytes is yet evaluated. Existing cell damage evaluation methods usually require cell staining, which are time-consuming and labor … bjs light house
A rapid and high content assay that measures cyto-ID …
Web20 hours ago · Autophagy was detected in lineage-negative BM cells, using Cyto-ID Autophagy Kit (#ENZ-51031-0050; Enzo, Farmingdale, NY). Because Cyto-ID uses the fluorescein isothiocyanate filter, Sca-1 was detected by allophycocyanin staining, whereas c-Kit cells were positively selected with c-Kit selection beads (#130-091-224; Miltenyi). WebJan 16, 2016 · Cyto-ID Green concentration contains 1 μl of Cyto-ID Green Detection Reagent in 1 ml cell culture medium. It was then mixed well and incubated for 30 min under standard tissue culture conditions at 37 °C, 5 % CO 2 in the dark. At the end of staining procedure, the Cyto-ID containing medium was washed with PBS. WebUsing Cyto-Tracers, cellular structures can be visualized in real-time by fluorescence microscopy without the use of chemical staining. You can also monitor the dynamic movement of a protein-of-interest in relationship to a given subcellular compartment or structure by labeling the protein-of-interest with separate fluorescent proteins. dating cesspool