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
logwood is but short, it is desirable that all the sections should begin
to be submitted to its action at the same time, otherwise some will
become more deeply stained than others. A good plan is to fill a small
porcelain jar (§ 14) with filtered water, and into this transfer the
sections. Whilst they are settling well down to the bottom, a mixture
must be prepared of half a drachm of Martindale’s solution (fresh) to
one ounce of distilled water, and everything got in readiness for its
immediate filtration. The water is now very gently to be poured off the
sections, and if care be exercised this may be done in such a manner as
to leave them undisturbed at the bottom, after removing almost every
drop of water. The diluted logwood fluid must now be _immediately_
filtered upon the sections, so that they may run no risk of becoming
dry. In the present instance the staining may be allowed to proceed for
about thirty minutes, and this will be found a convenient time for the
immersion of the general run of animal sections. If the logwood fluid be
not quite fresh, either a little more of it will have to be added to the
water, or the time of immersion must be prolonged until the desired
depth of color has been produced. It is well whilst the staining is
going on gently to shake the vessel occasionally, so that the sections
may not remain in a heap at the bottom, but all be as fully as possible
exposed to the action of the dye. When the staining is judged to be
complete, the logwood solution must be gently poured off, leaving the
stained sections at the bottom of the jar, when they should be quickly
covered with methylated spirit, which will _fix_ the colour. We shall
now be able to see if the coloration obtained be perfectly satisfactory.
If not deep enough, it is very easy again to submit them to the action
of the dye for a few minutes longer. If on the other hand, and as more
frequently happens, the coloration should be too deep, the excess of
colour may readily be removed by transferring the sections for a short
time into some diluted acetic acid prepared by adding five drops of the
glacial acid to an ounce of water. The action of this should be
carefully watched, and when the colour has been reduced to the desired
tint the sections may be retransferred to the methylated spirit.
Footnote 13:
Should the student, however, determine to prepare this solution for
himself, he will find a good formula for the purpose in Schäfer’s
“Practical Histology,” p 176. Note I.
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