Confocal microscopy experiments indicated that Nullbasic can disrupt Rev subcellular localization (Fig. 5).
Microscopy experiments show colocalization of both fluorescein and MG fluorescence.
As an interesting point, cross-sectional scanning tunneling microscopy (X-STM) experiments indicate substrate liquefaction below the droplets already at this low temperature [45].
The confocal microscopy and flow cytometry experiments indicated that mPEG-PLA-Phis micelles mediated efficient cytoplasmic delivery of Dox with the aid of poly l-histidine) mediated endosomal escapoly l-histidine
Both scanning electron microscopy (SEM) and in vitro permeability experiments indicated that the PM is the target of Mir1-CP [32], [34].
This in vivo electron microscopy data, combined with Western blotting and transfection experiments, indicates that native PLP co-localizes with mitochondria.
X-ray crystallography and electron microscopy (EM) structural studies in combination with biochemical experiments indicated that functional versatility of Mediator is intertwined with its structural heterogeneity.
Efflux defects for the UTI89 ΔhofQ and ΔgspD mutants were confirmed by fluorescence microscopy using green fluorescent protein-expressing strains, but these experiments indicated a delay in efflux rather than an absolute defect (R.K. and D.G.T. unpublished results).
Expression experiments indicated successful cloning.
In this report, confocal microscopy experiments and western blot assays indicated that the MDA-MB-231 breast cancer cell line did not express ERα, which was in accordance with its ERα-negative status.
Moreover, the determination of T N = 360 K and the negligible net magnetization at room temperature (Fig. 1b) clearly indicates that the electron microscopy experiments were performed within the antiferromagnetic regime.
