Work in stain in FDX

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Aug 6th, 2022
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How to work in stain in FDX

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The negatively charged cell wall of many microorganisms attracts the positively charged chromophore which causes the specimen to absorb the stain giving it the color of the stain being used. Positive staining is more commonly used than negative staining in microbiology.
There is little in the contents of most cells (which are 70% water by weight) to impede the passage of light rays. Thus, most cells in their natural state, even if fixed and sectioned, are almost invisible in an ordinary light microscope. One way to make them visible is to stain them with dyes.
Auxochromes are charged parts of chromogens that function as dyes to adhere stains to cells via ionizing groups. Most cells, including mammalian and bacterial cells, have negative charges on their membranes, which are drawn to by positively charged basic stains by exchanging ions.
When researchers apply stains to cells, the stains change the optical properties of some parts of the cell, but not others. This creates a contrast between the stained parts and the rest of the objects in the cell, allowing them to be seen more clearly than if the stain had not been applied.
Start by stripping off what you can (as described above), then seal the wood with a water-thin mix of de-waxed shellac and alcohol. Saturate the wood with the solution and wipe it off. Let it dry for 2 hours. Then switch to a 100 percent pigmented stain, such as Varathane (most stains are a mix of dye and pigment).
In a simple stain, dyes that are either attracted by charge (a cationic dye such as methylene blue or crystal violet) or repelled by charge (an anionic dye such as eosin or India ink) are added to the smear. Cationic dyes bind the bacterial cells which can be easily observed against the bright background.

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