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A9186

Sigma-Aldrich

Alcian Blue 8GX

BioReagent, suitable for detection of glycoproteins

Synonyme(s) :

Alcian Blue, Ingrain Blue 1

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About This Item

Formule empirique (notation de Hill):
C56H68Cl4CuN16S4
Numéro CAS:
33864-99-2
Poids moléculaire :
1298.86
Numéro C.I. (Colour Index):
74240
Numéro CE :
251-705-7
Numéro MDL:
MFCD00010720
Code UNSPSC :
12171500
ID de substance PubChem :
24891421
Nomenclature NACRES :
NA.32

Gamme de produits

BioReagent

Forme

powder

Composition

Dye content, ~50%

Technique(s)

electrophoresis: suitable

Adéquation

suitable for detection of glycoproteins

Chaîne SMILES 

[Cl-].[Cl-].[Cl-].[Cl-].CN(C)C(\SCc1ccc2c3nc(nc4n5[Cu]n6c(nc7nc(nc5c8cc(CS\C(N(C)C)=[N+](\C)C)ccc48)c9ccc(CS\C(N(C)C)=[N+](\C)C)cc79)c%10ccc(CS\C(N(C)C)=[N+](\C)C)cc%10c6n3)c2c1)=[N+](/C)C

InChI

1S/C56H68N16S4.4ClH.Cu/c1-65(2)53(66(3)4)73-29-33-17-21-37-41(25-33)49-57-45(37)62-50-43-27-35(31-75-55(69(9)10)70(11)12)19-23-39(43)47(59-50)64-52-44-28-36(32-76-56(71(13)14)72(15)16)20-24-40(44)48(60-52)63-51-42-26-34(18-22-38(42)46(58-51)61-49)30-74-54(67(5)6)68(7)8;;;;;/h17-28H,29-32H2,1-16H3;4*1H;/q+2;;;;;+2/p-4

Clé InChI

CKLBXIYTBHXJEH-UHFFFAOYSA-J

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Catégories apparentées

Description générale

Alcian Blue 8GX is a cationic phthalocyanine dye. It has an ability to interact with sulphated glycosaminoglycan. It is used as a counterstain to visualize histological tissue sections. In addition, alcian blue 8GX also aids in the in-situ quantification of marine biofilms produced by marine bacteria.

Application

Alcian Blue 8GX has been used:
  • for the quantification of sulphated glycosaminoglycan
  • to stain differentiated chondrocytes to access proteoglycan′s synthesis by these cells
  • to stain Multi-lineage differentiation of hemangioma-derived perivascular cells (Hem-PCs)
  • in histological staining to detect neutral and charged carbohydrate residues

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Anca Florentina Caliman et al.
Journal of hazardous materials, 144(1-2), 265-273 (2006-11-23)
The photocatalytic degradation of Alcian Blue 8 GX, a cationic copper phthalocyanine dye, has been investigated in aqueous suspensions containing the commercial catalyst TiO(2) P-25. The photodegradation of the organic molecule follows approximately a pseudo-first kinetic order, according to the
Inga Katharina Fuhrmann et al.
Acta histochemica, 117(3), 243-254 (2015-04-02)
The purpose of our study was to analyze the distribution of the major extracellular matrix glycosaminoglycan hyaluronan (HA), its receptor CD44 and cells which influence (re)modeling of the extracellular matrix (T- and B-cells, macrophages, endothelial cells) in menisci obtained from
A R Ribeiro et al.
Biointerphases, 7(1-4), 38-38 (2012-06-16)
Mutable collagenous tissues (MCTs) of echinoderms can be regarded as intelligent and dynamic biomaterials, due to their ability to reversibly change their mechanical properties in a short physiological time span. This mutability phenomenon is nervously mediated and involves secreted factors
Chloe Moreau et al.
Current biology : CB, 29(1), 35-50 (2018-12-18)
Limb position along the body is highly consistent within one species but very variable among vertebrates. Despite major advances in our understanding of limb patterning in three dimensions, how limbs reproducibly form along the antero-posterior axis remains largely unknown. Hox
J M Campos et al.
Regenerative biomaterials, 6(1), 49-59 (2019-02-12)
Development of synthetic bone substitutes has arisen as a major research interest in the need to find an alternative to autologous bone grafts. Using an ovine model, the present pre-clinical study presents a synthetic bone graft (Bonelike®) in combination with
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