These findings were similar to other studies [ 24, 42] and were also nicely demonstrated also with fluorescent markers, where implants showed direct apposition of new bone close to the implant and within the adjacent bone, especially in pure titanium or surface coated implants (PTST, TAN. TANNEW, CCTC, CCZTC).
Transcutaneous imaging of cells expressing green fluorescent protein and other fluorescent dyes has also been demonstrated with similar resolution to the luminescence-based imaging, but with less sensitivity owing to the greater background from autofluorescence and scattered excitation light [ 6].
The potential utility of the sensor for remote analysis is demonstrated with separations involving the CE analysis of charged fluorescent dyes, CE analysis of metal complexes based on in situ complexation and micellar electrokinetic capillary chromatographic analysis of neutral fluorescent compounds.
Analytical applicability of the film-Fe3+ complex for determining the levels of F− in environmental water samples has been successfully demonstrated by fluorescent analysis with satisfactory results.
As demonstrated by fluorescent immunostaining combined with confocal microscopy and flow cytometric techniques, this pathogen is present within neutrophils and eosinophil/basophil cells, as well as in the monocyte/macrophage cells previously implicated.
Multi-spectral images of 14 breast cancer specimens acquired before and after incubation with 2-NBDG demonstrated increased fluorescent signal in all of the malignant tissue due to increased 2-NBDG consumption.
The brain also demonstrated typical fluorescent intracytoplasmic inclusions by DFAT, with Russian (Kazan) and Centocor FITC-globulins.
As a proof of concept, we have demonstrated seven different fluorescent codes with only two different fluorescent dyes using T-DNA.
In conclusion, we have demonstrated lensfree fluorescent imaging of transgenic C. elegans over an ultra wide field-of-view of >2 8 cm2 with a spatial resolution of ∼10 µm.
Consistent with our findings, confocal image analyses demonstrated that green fluorescent protein-LPPl remains apically sorted, whereas green fluorescent protein-LPP3 co-localized with E-cadherin in cell-cell junctions and the basolateral domains of polarized MDCK cells [ 23, 33].
