Section Cutting and Staining: A practical introduction to histological methods for students and practitioners — John Shaqi
Section Cutting and Staining: A practical introduction to histological methods for students and practitionersColman, Walter S.
Science
Section Cutting and Staining: A practical introduction to histological methods for students and practitioners
Colman, Walter S.
Microscopy
Rub the carmine with a little water in a mortar, add the ammonia,
when the liquid will turn black. Gradually add the rest of the water,
rubbing it up all the time. It should be bottled, allowed to stand for
a few days, and then filtered, and a piece of camphor put in the bottle.
*Lithium carmine* resembles closely ammonia carmine in its staining
effects. It is usually a matter of individual preference which is
employed.
Carmine 2-1/2 grms. 10-1/2 grs.
Saturated aqueous solution
of lithium carbonate 100 c.c. 2 ozs.
Dissolve and filter.
Sections may be sufficiently stained in either of these fluids in from
three to five minutes, but more satisfactory results are to be obtained
by diluting with twenty times the bulk of distilled water, and leaving
sections to stain for twenty-four hours.
After staining in carmine the sections must be passed through a half
per cent. solution of acetic acid, in order to fix the carmine in the
tissues, as otherwise the water will dissolve the stain out.
*Borax carmine*--
(_a_) Borax 4 grms. 3 drachms.
Carmine 2 grms. 1-1/2 drachms.
Distilled water 100 c.c. 5 ounces.
Dissolve with the aid of heat and add slowly to (_b_).
(_b_) Alcohol 70 c.c. 3-1/2 ounces.
Distilled water 30 c.c. 1-1/2 ounce.
Allow to stand for a fortnight. Filter, and add a lump of camphor.
To use it, place sections, or the tissue in bulk, in it for from four
to twenty-four hours, according to size, and then transfer to alcohol
(seventy per cent.) containing a drop to the ounce of hydrochloric
acid, for twenty-four hours, and then wash thoroughly in water. The
tissue may then be placed in gum if it is to be frozen, dehydrated in
alcohol if paraffin or celloidin is to be employed.
Its advantage is that it is very diffusible, and so can be used
to stain tissues in bulk. It takes a considerable time to stain
sufficiently deeply, but there is little fear of overstaining.
It stains nerve-cells and axis cylinders brightly, and also the
connective tissue, bringing a sclerosed patch out very prominently.
*Alum carmine*:--
Alum five per cent. solution
in distilled water 100 c.c. 1 oz.
Pure carmine 1 grm. 4-1/2 grs.
Boil for twenty minutes. Filter. Add a few drops of carbolic acid.
In using this reagent it should be filtered into a watch glass, and
the sections placed in it for at least an hour. There is no fear of
overstaining, and they may be left all night. After they have been
stained they must be _thoroughly_ washed in water to remove the alum,
otherwise numerous crystals of it will be seen in the field when the
section is mounted. Sections may be mounted in Farrant’s solution or in
Canada balsam. The staining effect improves very much after the section
has been kept a few days.
Public-domain text, read in full here on John Shaqi.
Reviews
Reviews
No reviews yet
Be the first to share your thoughts on this work.
Join the Discussion
Join the discussion
Sign in to leave a comment or review.
Sign InorCreate an account