LESSON #1: PROPER TECHNIQUE OF SECTIONING TISSUE SAMPLES Flashcards
microtome used in the lab
Leica RM2125 RTS
sections produced by the Leica RM2125 RTS
0-60 um
initial sectioning: used at the very beginning of the secioning procedure to clear the tissue block (2 dots)
2.5 um
- dots used in todet to TRIM the tissue block enough to straighten it
2
final sectioning: used at the end of the sectioning procedure for the final cutting = final ribbons (1 dot)
10 um
temp of the floatation bath
5-10C below the melting point of the paraffin wax
utilized in order to affix the tissues to the glass slides prior to staining and viewing under the microscope
adhesives
most commonly used adhesive
Meyer’s Egg Albumin (1:1 concentration)
Meyer’s Egg Albumin composition
1ml egg white
1ml glycerine
added in the adhesive to PREVENT MOLDS; allow the slide to LAST FOR 3-4 MONTHS
phenol
also known as sectioning of cutting
microtomy
process where tissues are cut into uniformly thin slices
microtomy
paraffin embedded tissues are sectioned from - to facilitate microscopic studies
4-8 microns
basic instrument used to facilitate microscopic studies
microtome
microtome knives: 4 types
standard thick metal
thin disposable blades
glass knives
diamond knives
expensive knives; allows sharpening to your liking
standard thick metal knives
do the same job as the standard thick and probably better for a much lesser cost
thin disposable blades
these tissue sections are sectioned with GLASS OR DIAMOND KNIFE
embedded in plastic material: METHACRYLATE, ARALDITE, EPON
can section down to about 1 micron
glass knife
– microscopy thin sections are preferred sectioned to about 1/4 of a micron
electron
for sections of about 1/4 of a micron
diamond knife
artists of the laboratory
histotechnologists
common artifacts
tearing, ripping, holes, folding
helps REMOVE WRINKLES in sections
when sections are floated on a WARM WATER BATH