The Microscope. Its History, Construction, and Application 15th ed.: Being a familiar introduction to the use of the instrument, and the study of microscopical scienceHogg, Jabez
History
The Microscope. Its History, Construction, and Application 15th ed.: Being a familiar introduction to the use of the instrument, and the study of microscopical science
Hogg, Jabez
Microscopy; Natural history
By means of this stain the endothelial cells of the lymphatics, blood
vessels, &c., and the nodes of Ranvier, constrictions in medullary
nerves, are rendered visible. Sections of any of these may subsequently
be stained by logwood or carmine.
Several methods have been adopted for staining with gold chloride. Dr.
Klein’s and Professor Schäfer’s are among the best.
Dr. Klein’s method of showing the nerves of the cornea is as
follows:--Remove the cornea within fifteen minutes of death; place it
in a half per cent. chloride of gold solution for half an hour, or
an hour; wash in distilled water, and expose to the light for a few
days; in the meantime occasionally change the water. Then immerse it in
glycerine and distilled water, in the proportion of one to two; lastly,
place it in water, and brush gently with a sable pencil to remove any
precipitate, when it will be fit for mounting in glycerine. The colour
of the cornea should be grey-violet.
Schäfer adopts another method--a double chloride of gold and potassium
solution.
Osmic acid, first used by Schultze, is useful for the demonstration of
fatty matters, all of which it colours black; it is also valuable for
certain nerve preparations. Specimens should be allowed to remain in
a one or two per cent. aqueous solution of the acid from a quarter to
twenty-four hours, when the staining will be completed; but if it is
desired to harden specimens at the same time, they should remain in it
for some few days. Osmic acid does not penetrate very deeply, therefore
small portions should be selected for immersion. This is a useful stain
for infusorial animals.
Chloride of palladium, another of Schultze’s staining fluids, is used
to stain and harden the retina, crystalline lens, and other tissues of
the eye, the cornified fat and connective tissues remaining uncoloured.
The solution should be used very weak:--Chloride of palladium, one
part; distilled water, 1,000 parts. Specimens should be mounted in
glycerine at once, or further stained with carmine.
Dr. Schäfer employs a silver nitrate and gelatine solution for
demonstrating lung epithelium; this is made as follows:--Take of
gelatine ten grammes, soak in cold water, dissolve, and add warm water
to 100 cc. Dissolve a decigramme of nitrate of silver in a little
distilled water, and add to the gelatine solution. Inject this with
a glass syringe into the lung until distension is pretty complete.
Leave it to rest in a cool place until the gelatine has set; then cut
sections as thin as possible, place them on a slide with glycerine, and
expose to light till ready for mounting.
Of the double stains Mr. Groves prefers only those where the double
colour is produced by a single process--or stains in which one colour
is first employed, and then another. Single stains are picro-carmine,
carmine and indigo carmine, aniline blue and aniline red.
Picro-carmine is specially useful for staining sections hardened in
picric acid. It is prepared in several ways:--
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