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GHS132

Sigma-Aldrich

Hematoxylin Solution, Gill No. 1

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About This Item

Número MDL:
MFCD00078111
Código UNSPSC:
41116124
ID de substância PubChem:
24895389
NACRES:
NA.47

Formulário

solution

Nível de qualidade

500

prazo de validade

Expiry date on the label.

IVD

for in vitro diagnostic use

concentração

2 g/L

técnica(s)

microbe id | staining: suitable

pH

2.5-3.5

aplicação(ões)

hematology
histology

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

Oc1cc2C[C@@]3(O)COc4c(O)c(O)ccc4[C@H]3c2cc1O

InChI

1S/C16H14O6/c17-10-2-1-8-13-9-4-12(19)11(18)3-7(9)5-16(13,21)6-22-15(8)14(10)20/h1-4,13,17-21H,5-6H2/t13-,16+/m0/s1

chave InChI

WZUVPPKBWHMQCE-XJKSGUPXSA-N

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Aplicação

Gill No. 1 formulation is used as a progressive cytology stain. Used with hematoxylin and eosin staining.

Outras notas

2 g/L certified hematoxylin

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Warning

Frases de perigo

H302,H373

Classificações de perigo

Acute Tox. 4 Oral - STOT RE 2 Oral

Órgãos-alvo

Kidney

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Certificados de análise (COA)

Lot/Batch Number
SLCH6216
SLCC6882
SLBZ3495
SLBT9077
SLBS9853

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Our appreciation for the extent of Epstein Barr virus (EBV) transcriptome complexity continues to grow through findings of EBV encoded microRNAs, new long non-coding RNAs as well as the more recent discovery of over a hundred new polyadenylated lytic transcripts.
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Correct cardiac development is essential for fetal and adult life. Disruptions in a variety of signaling pathways result in congenital heart defects, including outflow and inflow tract defects. We previously found that WNT11 regulates outflow tract development. However, tissue specific
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Cytology & Cytodiagnosis

Brief information on the field of cytology, its role in cytodiagnosis and the use of standard and special stains for microscopic analysis to detect cellular abnormalities.

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