Sentence examples for microscopy to show from inspiring English sources
Here, we use quantitative time-lapse microscopy to show the spread of infectious cytoplasmic material between cells in the absence of lysis.
We used chemical biology approaches and live-cell microscopy to show that nuclear Cdk1-cyclin B1 promotes the translocation of Cdk1-cyclin B1 to the nucleus.
Fracture surfaces of failed specimens are examined using scanning electron microscopy to show micro- and macro-scale toughening/embrittling mechanisms.
In this study, we used live fluorescence microscopy to show that the C. elegans CAMSAP protein PTRN-1 localizes to puncta along neuronal processes, stabilizes MT foci, and promotes MT polymerization in neurites.
Using colloidal gold conjugates on immunodecorated cells, we used electron microscopy to show that AMI6 mAb targets an exposed antigen at the surface of A. minutum.
Images of the tablet surface and cross-section were characterized by scanning electron microscopy to show the formed pores and channels in the matrices.
Eichel and colleagues used a combination of microscopy techniques to show that transient engagement of the GPCR core, but not the C terminus, leads to prolonged accumulation of activated arrestin in CCSs.
(C) PC3 cells transfected transiently and stably with GFP-EN2 plasmid DNA were then co-stained with wheat germ agglutinin membrane stain (red), these were imaged and analysed using the confocal microscopy software to show co-localisation (40X magnification), the arrows on the images depict the cell through which the measurement was taken.
Electron microscopy fails to show storage material or enlarged lysosomes (not shown).
We have extended our life cell microscopy experiments to show that the different vesicular trafficking fates of recycling unliganded versus unidirectional trafficking of liganded EGFR are decided at the level of the EE.
We used transmission electron microscopy (TEM) to show that a high proportion of the isolates contain viable prophages and PCR targeting-specific myovirus genes, which suggested that there is a significant prophage diversity within these strains (Hargreaves et al. 2013).
