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Fluorescent illuminant

When crosslinking was first encountered, a number of colleagues advised us that the phenomenon was not likely to be of importance in a museum there, the natural or fluorescent illumination would consist only of those wavelengths that would pass through ordinary glass. We soon found, however, that, although... [Pg.184]

The manufacturer states that carmustine infusion solutions, packaged and stored in glass containers, are stable at room temperature (25°C) for eight hours when protected from intense UV-VIS radiation or normal fluorescent illumination (60 ft. candles = 645 lux), as determined by spectrophotometric and HPLC assays. [Pg.407]

Mitomycin C is intended for IV, intravesical, or ophthalmic use. The stability of reconstituted and diluted mitomycin solutions is pH dependent and is most stable between pH 7 and 8. According to the studies of Beijnen et al. (61) and Quebbeman et al. (62), the stability of mitomycin solutions are not markedly influenced by the container composition or room fluorescent illumination, even if exposed for several days. [Pg.413]

Infrared microscopes are commercially available from a number of companies worldwide, and operate much like conventional visible light microscopes. The IR radiation follows the same path as the sample iUumination Ught, so that IR micro-spectroscopy can be performed on the sample at the center of the viewing field. Because of their design, they are also equipped with a number of convenient methods for enhanced sample visualization. These include polarized light (visible and IR), fluorescence illumination and differential interference contrast (DIG), all of which are well known and frequently used to identify biological sample histology. [Pg.457]

Figure 14.8 (a) Visual image of Jurkat cells treated with the anti-Fas DX2 monoclonal antibody (mAb) under fluorescence illumination with the IR microscope. The green and red fluorescence signify early and late apoptosis, respectively (b) A comparison of the fingerprint region of untreated cells (AV7PF) (—) with those treated with the... [Pg.464]

Figure 10. Optical arrangement for single fluorophor imaging with a commercial inversion microscope and epi-fluorescence illumination. (Adopted from [64].)... Figure 10. Optical arrangement for single fluorophor imaging with a commercial inversion microscope and epi-fluorescence illumination. (Adopted from [64].)...
Fig. 3.5 Reflectance spectra of fresh beef during oxidation of oxymyoglobin to metmyoglobin obtained on a diode array spectrophotometer at 20 nm intervals means of over 100 samples wrapped in oxygen-permeable film and stored at <5°C under 1000 lux fluorescent illumination for one week. Fig. 3.5 Reflectance spectra of fresh beef during oxidation of oxymyoglobin to metmyoglobin obtained on a diode array spectrophotometer at 20 nm intervals means of over 100 samples wrapped in oxygen-permeable film and stored at <5°C under 1000 lux fluorescent illumination for one week.
Fig. 3.6 Progressive ehanges in lightness Z, hue angle /z and chroma C calculated from spectra of wrapped fresh beef stored at <5°C under 1000 lux fluorescent illumination during oxidation of surface oxymyoglobin to metmyoglobin. Fig. 3.6 Progressive ehanges in lightness Z, hue angle /z and chroma C calculated from spectra of wrapped fresh beef stored at <5°C under 1000 lux fluorescent illumination during oxidation of surface oxymyoglobin to metmyoglobin.
Selection plates with M2 seed are Incubated at 21 to 2 und r continuous fluorescent Illumination at about 80 uE m s. Herbicide resistant mutants should be easily recognizable after 3 to 10 days. Putative resistant plants are transplanted to soil and retested for resistance In the subsequent generations. [Pg.102]

I. Center and balance the output of the Hg bulb in the fluorescence illumination light path. [Pg.219]

The PSF in single-photon confocal and two-photon epi-fluorescence illumination systems... [Pg.108]

As the basis of solid-state lighting, white light-emitting diode (w-LEDs) are on the way to replace traditional incandescent and fluorescent illuminating sources due to the fact that they offer many attractive advantages including high efficiency. [Pg.461]

Optional) Mount the coverslip in Vectashield aqueous mounting medium and view the cells under fluorescence illumination to qualitatively assess cell loading of FDxLys. [Pg.32]

Plant growth conditions All A. thaliana plants were grown in controlled growth chambers, under continuous fluorescent illumination (150-200 pE m sec" ) at 22°C. All B. napus plants were grown under natural light supplemented with high pressure sodium lamps with a 16 hour photoperiod (16 h light/8 h dark), at 22°C, and a relative humidity of 25-30%. [Pg.408]


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See also in sourсe #XX -- [ Pg.176 ]




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