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B1064

Cibacron Blue 3G-A

Dye content ≥55 %, Powder

Synonym(e):

Cibacron Blue; 1-amino-4-[4-[[4-chloro-6-(2-sulfoanilino)-1,3,5-triazin-2-yl]amino]-3-sulfoanilino]-9,10-dioxoanthracene-2-sulfonic acid

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PackungsgrößeSKUVerfügbarkeitPreis
1 g
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€ 335,00

Über diesen Artikel

Empirische Formel (Hill-System):
C29H20ClN7O11S3
CAS-Nummer:
Molekulargewicht:
774.16
MDL number:
UNSPSC Code:
12171500
NACRES:
NA.47

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Produktname

Cibacron Blue 3G-A, Dye content ≥55 %

form

powder

Quality Level

composition

Dye content, ≥55%

color

dark blue

solubility

H2O: 10 mg/mL, blue

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

Nc1c(cc(Nc2ccc(Nc3nc(Cl)nc(Nc4ccccc4S(O)(=O)=O)n3)c(c2)S(O)(=O)=O)c5C(=O)c6ccccc6C(=O)c15)S(O)(=O)=O

InChI

1S/C29H20ClN7O11S3/c30-27-35-28(33-16-7-3-4-8-19(16)49(40,41)42)37-29(36-27)34-17-10-9-13(11-20(17)50(43,44)45)32-18-12-21(51(46,47)48)24(31)23-22(18)25(38)14-5-1-2-6-15(14)26(23)39/h1-12,32H,31H2,(H,40,41,42)(H,43,44,45)(H,46,47,48)(H2,33,34,35,36,37)

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Dieser Artikel
A315716030B5388
color

dark blue

color

dark blue

color

-

color

-

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

form

powder

form

powder

form

powder

form

powder

solubility

H2O: 10 mg/mL, blue

solubility

water: 1 mg/mL, blue

solubility

methanol: 0.01 g/10 mL, blue to very deep blue

solubility

water: 1 mg/mL, blue to very deep blue

composition

Dye content, ≥55%

composition

Dye content, ≥50%

composition

-

composition

Dye content, ≥60%

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

Application

When immobilized using an insoluble porous support matrix such as agarose, Cibacron Blue 3GA is used for affinity chromatography purification of enzymes.[1] This affinity has been attributed to a structural similarity between the dye and the natural ligands for proteins with cofactor binding domains.[2]

Biochem/physiol Actions

Cibacron Blue 3GA is an anionic anthraquinone dye. It acts as a P2-purinoceptor antagonist[3] and inhibits stimulus-evoked glutamate release by rat brain cortical tissue.[4] Cibacron Blue 3GA inhibits OXA-1[5] and OXA-2 β-lactamases[6] and was used to observe the binding of ligands to OXA-1 β-lactamase by monitoring tryptophan fluorescence.

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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W O Smith et al.
Plant physiology, 68(2), 443-446 (1981-08-01)
The binding of phytochrome to Cibacron Blue 3GA was utilized to develop a new affinity purification procedure for phytochrome. Brushite-purified phytochrome from rye (Secale cereale c.v. Cougar) was bound to agarose-immobilized blue dye in 0.1 molar potassium phosphate (pH 7.8)
S T Thompson et al.
Proceedings of the National Academy of Sciences of the United States of America, 72(2), 669-672 (1975-02-01)
A procedure is described to utilize blue dextran-Sepharose as an affinity chromatographic column specific for the super-secondary structure called the dinucleotide fold, which forms the binding sites for substrates and effectors on a wide range of proteins. The procedure can
G C Bennett et al.
British journal of pharmacology, 131(3), 617-623 (2000-10-04)
Evidence has previously been presented that P1 receptors for adenosine, and P2 receptors for nucleotides such as ATP, regulate stimulus-evoked release of biogenic amines from nerve terminals in the brain. Here we investigated whether adenosine and nucleotides exert presynaptic control
Kyle D Schneider et al.
Biochemistry, 48(26), 6136-6145 (2009-06-03)
Class D beta-lactamases hydrolyze beta-lactam antibiotics by using an active site serine nucleophile to form a covalent acyl-enzyme intermediate and subsequently employ water to deacylate the beta-lactam and release product. Class D beta-lactamases are carboxylated on the epsilon-amino group of
C Monaghan et al.
The Biochemical journal, 205(2), 413-417 (1982-08-01)
Although beta-lactamases do not require any nucleotide co-substrates, the OXA-2 type is inhibited competitively by Cibacron Blue 3GA, and by other anthraquinone dyes, including some simpler compounds with no side chain. The enzyme causes a red shift in the spectrum

Global Trade Item Number

SKUGTIN
B1064-1G04061832340036

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