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Merck
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Key Documents

MG500

Sigma-Aldrich

May-Grünwald Stain

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About This Item

MDL number:
MFCD00131580
UNSPSC Code:
41116121
NACRES:
NA.47

form

solution

Quality Level

500

shelf life

Expiry date on the label.

IVD

for in vitro diagnostic use

concentration

0.25 % (w/v) in methanol

application(s)

hematology
histology

storage temp.

room temp

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General description

May-Grünwald Stain has been employed to stain neutrophil granules and granulocyte inclusion bodies. May-Grünwald-Giemsa might be useful in the diagnosis of Malassezia folliculitis, a fungal mediated disorder.

Application

For use in the differential staining of cellular elements of blood

Preparation Note

Prepared with non-polychromed (non-oxidized) methylene blue and eosin Y.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Adlen Foudi et al.
The Journal of experimental medicine, 211(5), 909-927 (2014-04-09)
The zinc finger transcriptional repressor Gfi-1b is essential for erythroid and megakaryocytic development in the embryo. Its roles in the maintenance of bone marrow erythropoiesis and thrombopoiesis have not been defined. We investigated Gfi-1b's adult functions using a loxP-flanked Gfi-1b
Nuria Castro-Bravo et al.
Frontiers in microbiology, 8, 1405-1405 (2017-08-10)
An extracellular layer of exopolysaccharides (EPS) covers the surface of some
Historical hematology: May--Hegglin anomaly
Saito, Hidehiko and Kunishima, Shinji
American Journal of Hematology, 83(4) (2008)
Sunmi Park et al.
PLoS genetics, 13(9), e1006991-e1006991 (2017-09-15)
Patients with mutations of the THRA gene exhibit classical features of hypothyroidism, including erythroid disorders. We previously created a mutant mouse expressing a mutated TRα1 (denoted as PV; Thra1PV/+ mouse) that faithfully reproduces the classical hypothyroidism seen in patients. Using
Shirin Hasan et al.
Surgery, 162(4), 901-916 (2017-07-19)
Anemia of critical illness is resistant to exogenous erythropoietin. Packed red blood cells transfusions is the only treatment option, and despite related cost and morbidity, there is a need for alternate strategies. Erythrocyte development can be divided into erythropoietin-dependent and
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