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Further cell imaging has been realized successfully using FM-CPNs as staining label, and cytotoxicity was evaluated by the methyl thiazolyl tetrazolium (MTT) assay.
This comparison showed that Raman microscopy is capable of displaying the cell morphology; however, this is in contrast to hematoxylin and eosin staining label free and can therefore be applied potentially in vivo.
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After staining, labeled embryos were mounted in 90% glycerol and examined on an Olympus stereomicroscope (SZX-ILLD100, Tokyo, Japan).
L1 staining labels axon tracts.
Enhanced thioflavin-S staining labeled many neurons.
The mechanism by which the Gallyas-Braak staining labels NFT remains to be determined.
In untransfected HeLa cells, Zinquin staining labels small naturally occurring zinc-positive clusters.
Calcein-AM staining, labeling live cells, and TMRE staining, labeling all intact mitochondria, were performed with 1 μM Calcein-AM/50 nM TMRE/1 μg/ml H-33342 for 30 min at 37°C.
In pre-segmental larval stages, the first F-actin staining labels few, very delicate muscle fibers of the bodywall.
Caspase-3 staining labels intact undead cells in the posterior compartment (red in G, white in G ′). Labeling of the compartment with QUAS-Tomato is shown in green.
As a positive control for HLA-I-like molecule staining, labelling was performed in parallel with the mAb W6/32 (Parham et al., 1979).
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