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WS16

Wright Stain, Modified

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About This Item

UNSPSC Code:
41116121
eCl@ss:
42039003
NACRES:
NA.47
MDL number:
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form

solution

Quality Segment

shelf life

Expiry date on the label.

IVD

for in vitro diagnostic use

concentration

0.3%

pH

6.75-6.95 (25 °C)

application(s)

hematology
histology

storage temp.

room temp

General description

Wright stain is a polychromatic dye, used for microscopic examination of blood to identify different cell types.

Application

Wright Stain, Modified has been used in:
  • Phagocytosis assay and puberty.
  • Estrous cycle examinations.
  • Staining, to differentiate neutrophils.
Popular hematology stain used for differentially staining the cellular elements of blood. For dip, rack, and batch staining techniques.

Other Notes

Wright stain, 0.3%, buffered at pH 6.8 in methanol. Contains stabilizers and surfactant.

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This Item
WS32WG16WG32
concentration

0.3%

concentration

0.3%

concentration

0.4 % (w/v) in methanol (buffered at pH 6.8)

concentration

0.4 % (w/v) in methanol (buffered at pH 6.8)

application(s)

hematology
histology

application(s)

hematology
histology

application(s)

hematology
histology

application(s)

hematology
histology

form

solution

form

solution

form

solution

form

solution

Quality Level

500

Quality Level

500

Quality Level

500

Quality Level

500

IVD

for in vitro diagnostic use

IVD

for in vitro diagnostic use

IVD

for in vitro diagnostic use

IVD

for in vitro diagnostic use

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp


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signalword

Danger

Hazard Classifications

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

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

91.4 °F - closed cup

flash_point_c

33 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter



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Arginine and glutamine supplementation to culture media improves the performance of various channel catfish immune cells
Pohlenz C, et al.
Fish & Shellfish Immunology, 32(5) (2012)
Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice
Mercer, Rebecca E and Wevrick, Rachel
PLoS ONE, 4(1), e4291-e4291 (2009)
Rebecca E Mercer et al.
PloS one, 4(1), e4291-e4291 (2009-01-28)
MAGEL2 is one of several genes typically inactivated in the developmental obesity disorder Prader-Willi syndrome (PWS). The physiological consequences of loss of MAGEL2, but without the concurrent loss of other PWS genes, are not well understood. Gene-targeted mutation of Magel2



Global Trade Item Number

SKUGTIN
WS16-500ML04061837543586

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