Section-Cutting: A Practical Guide to the Preparation and Mounting of Sections for the Microscope, Special Prominence Being given to the Subject of Animal SectionsMarsh, Sylvester
Science
Section-Cutting: A Practical Guide to the Preparation and Mounting of Sections for the Microscope, Special Prominence Being given to the Subject of Animal Sections
Marsh, Sylvester
Microscopy; Microscopy -- Technique
14. _Carmine Staining._—In the case of animal sections, carmine is, as a
rule, to be selected, giving as it does most satisfactory and beautiful
results. Tissues may be stained with carmine by two different plans: in
the first, a strong solution is used, and the tissue subjected to its
action for a very short period only, whilst in the latter only very weak
solutions are employed, the time of immersion being considerably
prolonged. The rapid method, however, is not to be recommended, for the
strong carmine acts so powerfully upon the tissue as to give the various
elements comprising it no time, as it were, to exercise their power of
quantitive selection, but involves the whole in one uniform degree of
shadeless colour. By adopting the gradual method much better results are
obtained, each portion of the tissue being now at liberty to acquire its
own particular shade. Amongst the various formulæ for the preparation of
carmine fluid, none can be so safely followed as that devised by Dr.
Lionel Beale. It runs thus:—Place ten grains of the finest carmine in a
test tube, add thirty minims of strong liquor ammonia, boil, add two
ounces of distilled water, and filter; then add two ounces of glycerine,
and half an ounce of rectified spirit—this solution ought to be kept in
a well stoppered bottle. The best vessels in which to stain sections are
small jars of white porcelain, capable of holding about two fluid
ounces, and furnished with lids—they are much preferable to beakers or
watch glasses, for owing to the white background which they afford it is
very easy to watch how the staining is proceeding. The carmine solution
which we have just described is both too strong and of too great density
to be used in its pure state. It will, therefore, require to be diluted
with distilled water before use—the most useful degree of dilution being
attained by adding one part of stain to seven of water. Sections may be
placed in this solution for twenty-four hours, in which time they will
usually be found to have acquired a sufficient depth of colour. If,
however, the tissue be unusually difficult to stain, the time of
immersion may be doubled, or still further prolonged, without detriment
to the section.
[Illustration: SECTION SPOON.]
Public-domain text, read in full here on John Shaqi.
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