Not exact matches
Grape - like structures of viral replication territories in the nucleus of a human
cell visualized
by click - chemistry and immuno -
fluorescence confocal
microscopy.
Recombinant proteins containing tetracysteine tags can be successively labeled in living
cells with different colors of biarsenical fluorophores so that older and younger protein molecules can be sharply distinguished
by both
fluorescence and electron
microscopy.
Our success in these areas is complemented
by our substantial investment in cutting - edge facilities for nuclear magnetic resonance, protein crystallization, X-ray crystallography, transgenics, histochemistry, electron
microscopy, confocal
microscopy, and
fluorescence activated
cell sorting.
By developing a new
fluorescence microscopy - based technique, the researchers were able to measure how long it takes proteins to move over distances ranging from 0.2 to 3 micrometres in living
cells.
Cell viability is monitored
by trypan blue exclusion and purity of the preparations is routinely assessed
by morphology, as well as specific staining (ED2 (rat) or F4 / 80 (mouse)-RRB-
by flow cytometry or
fluorescence microscopy.
Responses were correlated to calcium release in cultured rat uterine smooth muscle
cells measured
by fluorescence microscopy.
A Postdoctoral Research Associate Position is available funded
by the Wellcome Trust, to study the nanoscale organisation of human immune
cell surfaces
by super-resolution
fluorescence microscopy.
Cells are visualized
by phase contrast (left) and
fluorescence microscopy (right).
With two - photon
fluorescence microscopy Professor Denk could perform two tasks simultaneously: stimulate the photoreceptors of an isolated rabbit retina
by moving a light stimulus over it in one direction, and at the same time, record the
fluorescence from the individual dendrites of starburst amacrine
cells.
Intestinal permeability was assessed
by Ussing chamber; epithelial
cell (EC) ultra-structure
by electron
microscopy; RNA expression of genes coding for junctional proteins
by Q - real - time PCR; immune response
by in - vitro antigen - specific T -
cell proliferation and cytokine analysis
by cytometric bead array; intestinal microbiota
by fluorescence in situ hybridization and analysis of systemic antibodies against intestinal microbiota
by surface staining of live bacteria with serum followed
by FACS analysis.
In cases of neonatal mortality, the diagnosis typically is made postmortem with virus isolation from fresh lung, liver, kidney, and spleen
by cell culture techniques and subsequent identification
by PCR and sequencing, transmission electron
microscopy, immunofluorescence, or
fluorescence in situ hybridization.