Nettet28. apr. 2014 · We report a general strategy to create small-molecule fluorescent probes for the nucleus in living cells. Our strategy is based on the attachment of the DNA-binding Hoechst compound to a fluorophore of interest. Using this approach, simple fluorescein, BODIPY, and rhodamine dyes were readily converted to nov In celebration of Seiji … Nettet24. mar. 2024 · Nakamura, A. & Tsukiji, S. Ratiometric fluorescence imaging of nuclear pH in living cells using Hoechst-tagged fluorescein. Bioorganic & Medicinal Chemistry Letters 27 , 3127–3130 (2024).
Hoechst tagging: a modular strategy to design synthetic …
NettetFor all dyes the H2B-GFP chromatin label and DNA staining were imaged in interphase and mitotic cells. The three fixed-cell dyes TOTO-3, TOPRO-3, and PI were imaged with or without RNAse digestion. Dye concentrations are as listed in Table 1. For Hoechst and DRAQ5, only live cell images are shown. Nettetfor 1 dag siden · Cells were incubated for 15 minutes prior to live cell imaging. Stained cells were visualized using a Nikon A1R Confocal Microscope (SickKids Imaging Facility, Toronto) with excitation wavelengths of 405 and 568 to detect signals from Hoechst 33342 and CSRBnps respectively. microchip information pet
Super-resolution 3D live cell imaging Nature Methods
NettetIn this study, kinetic live cell imaging was used to monitor cAMP levels in HEK293 cells expressing a cAMP biosensor while stimulating D2, M2R, and β2 receptors. Furthermore, automated image analysis was used to characterize Gs- and Gi-dependent changes in cAMP levels over time and determine pharmacological dose-responses. Read more. Nettet14. aug. 2024 · Modulation of the chromatin density of living NIH/3T3 cells stained with Hoechst 34580 and evaluation by fluorescence lifetime imaging microscopy (FLIM): … NettetHoechst 33342 for 72h live imaging, is it ok ? Question. 4 answers. Asked 8th May, 2016; ... I am going to use a live cell imaging platform and it would be a 72-96 hrs long experiment. microchip internship