AGf~ICULTURAL RESEARCH, PUSA.
AGf~ICULTURAL RESEARCH, PUSA.
AGf~ICULTURAL RESEARCH, PUSA.
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STAINING METHODS 149<br />
the top of the Bunsen flame for a few seconds so that<br />
the slide becomes hot. Care must be taken not to<br />
char the film, and when the slide is just too hot to be<br />
borne on the back of the hanel, fixation is complete.<br />
Films on cover-slips require a minimum of time for<br />
fixing owing to the thinness of the glass. The covcrslips<br />
may be held by means of Comet's forceps.<br />
With solid material, such as cultures on agar, etc.,<br />
it is necessary to place a loopful of clean "IJater on the<br />
slide. The loop is t.hen sterilised and a minute quantity<br />
of material, obtained by just touching the growth, is<br />
transferred to the drop, thoroughly emulsified, and<br />
the mixture is spread evenly on the slide. The resulting<br />
film is fixed and dried as above. Beginners are<br />
very apt to take more material than necessary from<br />
the cultnrc and thus make too thick jilms_<br />
STAINING<br />
The method of staining varies with the nnture of<br />
the prcparation (film or section).<br />
FILMS<br />
'fhe stains arc poured directly or filtered on to the<br />
slide. W hen staining is completed, the dye is washed<br />
off with water and the slide is allowed to dry in the<br />
vertical position or is placed between two sheets<br />
of 'white fluftless blotting-paper or filter paper. The<br />
drying of the film is completed over the Bunsen name.<br />
Such stained films may be monnted in Canada balsam<br />
under a cover-slip, or may be examined ulllllounted<br />
with the oil-immcrsion lens, a small drop of eedarwood<br />
oil being placed directly on the film. If it is<br />
desired to mouut the preparation later, the oil can<br />
be removed with xylol.<br />
TISSUE SECTIONS<br />
. The scetions being embedded in parafllll (1,idc p.177),<br />
it is neeessary to rentoye the paraffin so that a watery<br />
stain may penetrate. 1'he paraffm is first removed