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At the electron microscopy level, Hfq-MT molecules were visualized as small electron-dense particles in thin-sections of bacteria expressing the Hfq-MT fusion protein (Fig. 2).

The resulting double-stranded heteroduplex molecules were visualized by silver staining.

Immobile single fluorescent molecules were visualized by an objective-type TIRF microscope.

Molecules were visualized alongside the original ligand VPL57 and the 2D interaction plots generated.

Single molecules were visualized by prism-type TIRF microscope and analyzed using Matlab scripts (https://github.com/vasuagg/SiMPull_Analysis).

Three Ub molecules remained on the K11 and K48 homotypic chains, while four Ub molecules were visualized on the heterotypic chains.

The movement of intertwined loops, or plectonemes, along a twisted DNA molecule was visualized.

Briefly, motility assays were assembled using flow chambers, and fluorescently labeled dynein molecules and microtubules were visualized by TIRF microscopy (Qiu et al., 2012; Reck-Peterson et al., 2006).

Single-molecule FRET images were visualized by a total internal reflection fluorescence microscope equipped on an inverted type microscope (IX70 or IX71; Olympus), as previously described (Funatsu et al, 1995; Taguchi et al, 2001; Mori et al, 2007).

Highly extensible Escherichia coli DNA molecules in planar extensional flow were visualized in dilute solution by fluorescence microscopy.

Molecules retained on the surfaces were visualized by reading the spots of each array in a SELDI-TOF-MS reader (PBSII; Ciphergen).