One embodiment of the present disclosure is directed toward an epifluorescence microscope.
In this case, it is no longer possible to use the term “epifluorescence”.
Positions of hybridization of a target nucleic acid are determined by, e.g., epifluorescence microscopy.
Disclosed is a microscope for conventional fluorescence (epifluorescence) microscopy and total internal reflection microscopy.
Observe the slides immediately with a microscope fitted for epifluorescence microscopy at 630 or 1000 × magnification under immersion oil.
All of the embodiments may be used for epi-fluorescence microscopy.
For instance, both epifluorescent and total internal reflection (TIR) methods may benefit from the techniques of the present invention.
Epifluorescent imaging of the three components in a dividing human cancer cell.
The epifluorescent imaging system comprises a metal halide lamp comprising a gas discharge tube (14), fitted in the fitting (12).
The approach is based on a high-speed pin printer and imaging with an epi-fluorescence microscope/charge coupled device detector.
The method as claimed in claim 11, in which said step b) is carried out by epifluorescence microscopy.
The apparatus may be configured for time-lapse photomicroscopy, transmission photomicroscopy, reflection photomicroscopy, epifluorescence photomicroscopy, or infrared photomicroscopy.
1 top-down microscope (ZEISS Axioscope.A1) with LED epifluorescence, Sony dark-fluorescence digital camera, and Dell workstation
An epifluorescence microscope is used to observe, four days later, the development of dendrites and magnificent neurons with the characteristic form.
The optical instrument (10) may be an epifluorescence microscope (12) for use in observing an image formed from light from an object (44) under illumination by a light source (14).
Soon after emergence, anesthetize G1 individuals using CO2 and check for transformation events under an epifluorescence stereomicroscope.
A fibre optic epi-fluorescence imaging system in which the optical fibres are rearranged so that the system can be used for measuring luminescence samples.
With epifluorescent and confocal microscopy, it is now possible to visualize specific microorganisms directly in their environment, for example, in biofilms.
Examine the stained smear with an epifluorescence microscope at 450 nm under oil immersion at a magnification of 600 to 1000 using an oil- or water-immersion objective.
Glioblastomas are the most common tumors of the central nervous system Image taken using a Zeiss Axioimager Z1 widefield epifluorescence microscope.
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