The stain has a similarity with
loeffers alkaline methylene blue. They are used for demonstration of Anthrax
bacilli structure in the blood.
| LABORATORY PROCEDURE FOR POLYCHROME METHYLENE BLUE STAIN |
Preparation. the same with loeffer
alkaline methylene blue. After that distribute in the battle, record date
label.
| LABORATORY PROCEDURE FOR POLYCHROME METHYLENE BLUE STAIN |
Shake frequently before it can be
ready for used, it takes several months, but it can be foster by treating with
chemical.
Procedure: is the same of that of
loefler alkaline methylene blue.
| LABORATORY PROCEDURE FOR POLYCHROME METHYLENE BLUE STAIN |
ALBERT STAIN
This stain is use for
demonstration of corynebacterium diphtheriae, in microbiology laboratory. It
has two solutions one and two.
SOLUTION PREPARATION
Toluidine blue 1.5g
Malachite green 2 .0g
Ethyl acetic acid 10ml
Ethyl alcohol -95% 20ml
Distilled water 100ml
METHOD OF PREPARATION
First dissolved tuluidine blue,
and malachite alcohol then add water and acetic acid, leave the solution at
room temperature for 24h and filter, record date label and store.
2 SOLUTIONS
Iodine 6g
Potassium iodide 9g
Distilled water 900ml
METHOD OF PREPARATION
Dissolved potassium iodide into
50ml of water and iodine dissolved and make up the total volume by adding
water.
PROCEDURE
1 prepares a smear from loeffer
serum culture between 18-24h of the test organism and allowed to dry and fix
with gentle heat.
2 Apply solutions one for 3-5
minutes
3 Wash with water and blot carefully.
4 Apply solutions 2 for 1 minute.
5 Wash with water and blot
carefully and dry by gentle heat.
6 Take to microscopy for
examination.
Result: Granule stained bluish
black the remaining organism stained green.
Pugh Stain: This stained is also
used for the examination of the structure of Carynebacterium diptheriae.
SOLUTION
Taluidine blue 1g
Ethyl alcohol absolute 20ml
Acetic acid glacial 50ml
PREPARATION
Mix acetic acid with distilled
water and add toliudine blue and dissolved in ethyl alcohol filter record date
and label and store.
PROCEDURE
1 Prepare a smear from serum
culture between 18-24hour of loeffer test organism allowed to dry and fix by
gentile heat.
2 Apply solutions for 1-3 minute
3 Wash with water blot carefully
and dry by gentle heating.
Examine with microscope.
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