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BISC209: Preparing a bacterial smear slide: Difference between revisions
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BISC209: Preparing a bacterial smear slide (view source)
Revision as of 11:39, 5 January 2010
, 5 January 2010→Preparing a bacterial smear slide
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Preparing a bacterial smear slide is useful for microscopic examination of dead bacterial cells.<br> | Preparing a bacterial smear slide is useful for microscopic examination of dead bacterial cells.<br> | ||
1. Place a very small loopful of | 1. Place a very small loopful of deionized water on the slide (you can use the deionized water bottle on your bench-remove the cover and dip your loop in since sterility is not required for this step).<br> | ||
''Note:'' If the bacterial smear is being made from a broth, simply place a loop or two of the broth culture on the slide and spread, do not use additional water.<br> | ''Note:'' If the bacterial smear is being made from a broth, simply place a loop or two of the broth culture on the slide and spread, do not use additional water.<br> | ||
2. Flame the loop, cool and touch it to the colony or slant growth and place the now contaminated loop into the drop. Use large circular motions to spread the drop to about the size of a quarter over the slide.<br> | 2. Flame the loop, cool and touch it to the colony or slant growth and place the now contaminated loop into the drop. Use large circular motions to spread the drop to about the size of a quarter over the slide.<br> | ||
3. Reflame the loop.<br> | 3. Reflame the loop.<br> | ||
4. Be sure all the water on the slide has evaporated before proceeding to heat fixation. <br> | 4. Be sure all the water on the slide has evaporated before proceeding to heat fixation. <br> | ||
5. Heat fix ( | 5. Heat fix (to kill and attach organisms to slide) by rapidly passing the slide (smear side up) through a flame 3 times. Use a slide holder and avoid contact with hot glass.<BR><BR> | ||
With practice it is more efficient to put multiple samples on one slide. | With practice it is more efficient to put multiple samples on one slide. When staining multiple smears on one slide you must be careful to apply the staining reagents so they cover all smears evenly and for the same amount of time. Label the slide with a graphite pencil in the ground glass section on the far left of the slide since the reagents used in staining (such as the decolorizer in the Gram stain) can remove your labels if you use pen or wax pencil. By convention, labels (top to bottom) match smears (right to left).<BR> | ||
An example of a multiple smear labeled slide: <BR> | An example of a multiple smear labeled slide: <BR> | ||
[[Image:gramSLIDE2-2.jpg]] | [[Image:gramSLIDE2-2.jpg]] | ||
