Cyto-id staining
Webtook advantage of Cyto-ID, a uorescent dye for selective staining of autophagosomes [45–47], in two ways: First, we conducted double-labeling ow cytometry with Cyto-ID and the live-cell-permeant DNA marker DRAQ5, allowing for simultaneous monitoring of autophagy and cell cycle phases. Second, we developed a Cyto-ID-based ow-cyto- WebJul 21, 2024 · Autophagosome staining was then performed using the Cyto-ID reagent, and Hoechst 33342 as a counterstain. 2 × 2 composite images were taken on a Zeiss AxioObserver motorized microscope at a ×10 ...
Cyto-id staining
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http://biopioneer.com.tw/?p=41115 WebJan 30, 2013 · Determination of autophagy (Cyto-ID staining) Flow cytometric analysis of Cyto-ID Green Detection Reagent stained cells was performed according to manufacturer's protocol (Cyto-ID Autophagy Detection Kit, ENZ-51031-K200, Enzo Life Sciences). In brief, harvested cells were washed with PBS, stained with Cyto-ID in indicator-free medium …
WebJan 1, 2014 · The intensity of Cyto-ID fluorescence in RTCs did not increase after incubation with rapamycin for 3 h compared to the vehicle control or even exhibited a tendency to decrease (Fig. 5, a and e). ... WebApr 14, 2024 · For CYTO-ID staining, cells were incubated for 30 min in N2B27 containing 2 μl/ml of CYTO-ID Green. Cells were then washed and fixed with 4% paraformaldehyde and processed for immunofluorescence imaging as above. Wide-field microscopes used: Leica DMRD upright fluorescence microscope fitted with a Leica DFC450 C camera 5 …
WebNov 5, 2024 · After staining with Cyto-ID, autophagosomes were quantified measuring an increase in green fluorescence (FL1) using flow cytometry (** p < 0.01, ***p < 0.001 compared to the serum only group). 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 ).
WebCyto Prep Technician - Stony Brook Pathology UFPC. Location: Stony Brook, NY. Schedule: Per Diem. Days/Hours: As needed. Summary. At Stony Brook Medicine, a Cyto Prep Technician is a valuable ...
WebWe first verified that the Cyto-ID dye specifically labels autophagic compartments with minimal staining of lysosomes and endosomes. We then developed a new Cyto-ID fluorescence spectrophotometric assay that makes it possible to estimate autophagy flux based on measurements of the Cyto-ID-stained autophagic compartments. florida gator motorcycleWebJan 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. florida gator predictions 2023WebJun 26, 2024 · LysoTracker + (top) and CYTO-ID + (bottom) vesicles are shown in the background of MAP2 neuronal staining (n = 3 biological replicates). Scale bars are 25 μm. Scale bars are 25 μm. Source data ... great wall epsomWebCyto-Last™ Buffer is specially formulated for the storage of cytokine producing cells. When used, staining of intracellular and/or extracellular targets for flow cytometric analysis can be delayed for up to two weeks. Cells should be stored at 4°C during this time. This unique buffer ensures cells maintain a background staining signal equal ... greatwall engine assy factoryWebIn this work, the Cyto-ID dye is shown to colocalize with RFP-LC3 in starved HeLa cells, which further validate the specificity of the dye. The developed image-based autophagy … florida gators 2023 baseball scheduleWebNov 25, 2024 · Co-staining of endogenous pATG16L1 s278 and LC3B revealed a partial colocalization and upregulation of puncta with both … florida gators away jerseysWebUsing 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. great wall erie