In simple staining the bacterial smear stained with single dye or reagent which bring the distinctive contrast between organism and its background. PROCEDURE: 1 Prepare bacterial smear by placing loopfull culture of bacteria on slide. 2 Allow the slide to dry and heat fix it over flame. Do not heat extreamly, it can demage the shape or structure of bacteria. 3 Now flood the smear with methylene blue for 1-2 minutes. 4 Gently wash the smear with distill water to remove excess stain and dry it slowly with tissue paper. 5 Examine the slide in 100x or oil-immersion for the morphology of bacteria.
It is the use of single stain or dye to create contrast between bacteria and the background.
The purpose of simple staining is to elucidate the morphology and arrangement of bacterial cells. (Cappuccino, Sherman: Microbiology, a Laboratory Manual).
The function of simple staining is to enhance visual contrast to specimens. This is done to transparent specimens when using a microscope.
It acts as the mordant to soften the mycolic acid so that the stain can penetrate the cell.
Perhaps Gram Staining? Steps are as follows: 1. Crystal Violet, 2. Iodine, 3. Decolorizer, 4. Safrinin
acid fast staining or Ziel Neelson staining for observing Mycobacteria tuberculosis or Koch bacilli from sputum sample.
fluorescein staining
capsule does not gets stained it appears to be colourless when stained using manewals staining procedure
Fontana silver staining.
It acts as the mordant to soften the mycolic acid so that the stain can penetrate the cell.
Perhaps Gram Staining? Steps are as follows: 1. Crystal Violet, 2. Iodine, 3. Decolorizer, 4. Safrinin
not sure
Carbohydrate demonstration methods. Demonstrates Staining mechanisms and technical comments.
differential staining is a staining technique used to stain colorless bacteria against a dark background.
Gram, Ziel-Nielsen
flagellar stain
The bacterial smear will wash away during the staining procedure. This is avoided by heat fixation, during which the bacterial proteins are coagulated and fixed to the glass surface.
This is simply important in order to have accurate staining results. If this is not followed, the process of the staining will result to false positives or false negatives.
to detect bacterial stracture
acid fast staining or Ziel Neelson staining for observing Mycobacteria tuberculosis or Koch bacilli from sputum sample.