Sentence examples for microscopy we monitored from inspiring English sources

Using immunofluorescence microscopy, we monitored the transport of the hybrid GP5 and M proteins to the Golgi complex, which depends on their heterodimerization and is a prerequisite for virus assembly.

Using live cell microscopy we monitored migration of cells into wounds.

Using timelapse fluorescence microscopy, we monitored anaphase spindle dynamics in PtK2 cells stably expressing GFP-α−Tubulin [36].

Using time-lapse confocal microscopy, we monitored STIM1-GFP redistribution in hippocampal neurons in response to TG-induced store depletion (Figure S1 and Movie S1).

Using live-cell microscopy, we monitored adhesion of these inducible strains to ME180 cells over time, starting in the absence of induction and followed by the addition of IPTG after 2 hours of bacteria-cell interaction (Figure 3, Video S1 and Video S2).

Using epi-fluorescence microscopy, we monitored the regrowth of capillaries in the PDT treated area.

First, using in vivo two-photon microscopy (TPM), we monitored the migration of fluorescence-labeled T cells into the ankle joints and joint-draining lymph nodes (JDLNs) of syngeneic severe combined immunodeficient (SCID) mice during the course of the adoptive transfer of PGIA.

By confocal microscopy, we then monitored the presence of dotted green fluorescence that is typical of active autophagosome formation.

By carrying out single-molecule atomic force microscopy refolding experiments, we monitored kinetic evolution processes of these different conformers.

To assess the extent of migration by laser confocal microscopy live imaging, we monitored the mobility of 5-chloromethylfluorescein diacetate (CMFDA -labeled BMM CMFDA -labeledemotaxis chamBMMs with media alone or culturedned from infechemotaxisglia in the presenchamberssence of astrocytes.

Using high resolution transmission electron microscopy and Raman spectra, we monitor the structure evolution of tribofilms and friction coefficient drop during running-in.