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Neuro2a cells transfected with shRNA expression vectors were visualized by GFP.
The resulting shape vectors were visualized by generating synthetic skull outlines in Past, version 3.0.
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The derived flow vectors were visualized as color-coded arrows, overlaid on a compounded B-mode image, whose pointing direction corresponded to the estimated vector angle, and whose arrow length and color were pegged to the vector magnitude.
To examine this possibility, HeLa cells were co-transfected with MT-RFP and either MULAN or the vector control, and microtubules were visualized by staining with α-tubulin antibody.
Immuno-deposits were visualized by using the avidin biotin peroxidase kit (Vector).
BAC-contigs arranged on the 21 G. aculeatus chromosomes were visualized by passing coordinates to a vector graphics application (CorelDRAW version 11, Corel corp., Ottawa, Canada).
Nuclei were visualized by counterstaining DNA with 4',6-diamidino-2-phenylindole (DAPInc.Vector LaBurlingamenCA, BUSAingame, CA, USA).
The staining's were visualized by using an ImmPact™ DAB substrate kit (Vector).
According to the manufacturers' instructions, the PCR products were visualized by ethidium bromide staining and subcloned into the pMD19-T vector.
Liquid droplets were visualized by DIC microscopy.
Nuclei were visualized by DAPI (blue).
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