Title Description
REF No 5025
Purpose It is used for light microscopic examination of blood cells, lymphohemopoietic tissues and parasites in tissue sections.
Ingredients Glycerol, Methylene blue, Eosin Y, Methanol, Giemsa stain, Buffers.
Working Principle May Grunwald-Giemsa stain (MGG) is a Romanowsky stain routinely used for staining air-dried cytological smears, blood and bone marrow smears. Cytological preparations from FNAC and serous fluids are normally processed with May Grunwald-Giemsa stain. It is useful for examining cellular morphology and is superior to PAP staining for examining the cytoplasm, granules, vacuoles and basement membrane.
The working principle of MGG stain is the same as other Romanowksy stains. Polychromatic Romanowksy stains contain different proportions of methylene blue (and reagent-related thiazine dyes such as azure B) as the cation (+ highly charged, basic) component and eosin Y as the anion (- highly charged, acidic) component. . The combination of cation and anion components produces the well-known Romanowsky effect or metachromasia.
The solvent methanol initially stabilises the cells. The basic stains carry net positive charges; consequently they stain nuclei (due to the negative charges of the phosphate groups of DNA and RNA molecules), basophil granulocyte granules and RNA molecules of the cytoplasm. Eosin carries a net negative charge and stains red blood cells and eosinophil granulocyte granules.
Warnings, Precautions, Recommendations Highly flammable liquid and vapour. Toxic if swallowed, in contact with skin or inhaled. Causes damage to organs. Keep away from heat/sparks/flame/hot surfaces. - No smoking. Wear protective gloves/protective clothing/eye protection/face protection. IF IN CONTACT WITH SKIN (or hair): Immediately remove all contaminated clothing. Rinse skin with water/shower. In case of exposure: Call NATIONAL POISON ADVICE CENTRE TELEPHONE 114 or doctor/physician
Application Application of the staining method:
-Cover the preparation with 10 drops of "A-May-Grünwald solution". After 3 minutes proceed to the next step without pouring the reagent.
-Add 10 drops of "Buffer working solution" to the reagent in the preparation. Mix the two reagents by blowing or small oscillations. After 6 minutes, remove the reagent by shaking the slide.
-Immerse the preparation in a beaker of "Buffer working solution". After 1 minute, remove the slide and shake off the reagent.
-Immerse the preparation in a beaker of "Giemsa working solution". After 20 minutes, remove the slide and shake off the reagent.
Air-dry the smear and examine under a microscope with an immersion objective. Dehydrate the tissue section, clean, cover with synthetic resin and examine under the microscope.
Theoretical Results
Neutrophil cytoplasm

Shaded dirty pinkish

Lymphocyte cytoplasm

Sky blue

Eosinophil cytoplasm

Blue

Plasmodium cytoplasm

Blue

Monocyte cytoplasm

Pale blue

Eosinophil granules

Red to purple

Basophil granules

Dark purple or blackish

Neutrophil granules

Light purplish

Leukocyte nuclei

Reddish purple

Plasmodium chromatin

Red

Platelets granules

Violet purple

Erythrocytes

Reddish

Related Media
Shelf Life 2 years
Shelf Life After Opening the Lid
Storage Temperature 15-25°C
pH (at 25°C)
Transportation Information
Ordering and Packaging Information
Order No Unit Volume Packaging Type Quantity in a Box Quantity in a Parcel
445025050050 Piece 50 mL 50 ml, White Bottle with HDPE Dropper 1 kit 20 kits
445025020250 Piece 250 mL 250 ml, PP White Bottle with Dropper 1 kit 15 kits
445025020500 Piece 500 mL 500 ml, HDPE White Bottle 28 mm 1 kit 6 kits

Keywords MGG, Giemsa Stain, May-Grunwald Giemsa Stain
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