what is light microscopy?
light microscopy is conventional bright-field microscopy and more specialized applications like fluorescence, phase-contrast, confocal, and polarizing microscopy are all based on the interaction of light with tissue components and are used to reveal and study tissue features.
what are the types of light microscopy?
what does bright field microscopy include?
what are the optical components of the bright field microscope
what is the resolving power of the bright field microscope
the resolving power of the microscope is 0.2um, meaning objects smaller or thinner than this cannot be distinguished (e.g. a ribosome, membrane, etc.). Likewise if two objects are closer than this together they cannot be distinguished.
what is virtual microscopy?
what is meant by the term flourescence?
When certain cellular substances are irradiated by light of a proper wavelength, they emit light with a longer wavelength— a phenomenon called fluorescence
how does flourence microscopy work?
what are fluorescent compounds used for?
Fluorescent compounds with affinity for specific cell macromolecules used as fluorescent stains. e.g Acridine orange, which binds both DNA and RNA
coupling compounds such as fluorescein to molecules that will specifically bind to certain cellular components and thus allow the identification of these structures under the microscope
what is phase contrast microscopy?
how does phase contrast microscopy work?
based on the principle that light changes its speed when passing through cellular and extracellular structures with different refractive indices
These changes are used by the phase-contrast system to cause the structures to appear lighter or darker in relation to each other.
what is differential interference contrast microscopy?
A modification of phase-contrast microscopy, with Nomarski optics, which produces an image of living cells with a more apparent three-dimensional (3D) aspect
what is confocal microscopy?
-a small point of high-intensity light, often from a laser
a plate with a pinhole aperture in front of the image detector. The point light source, the focal point of the lens, and the detector’s pin- point aperture are all optically conjugated or aligned to each other in the focal plane (confocal), and unfocused light does not pass through the pinhole