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C9210

Sigma-Aldrich

Cyanogen bromide-activated Agarose

lyophilized powder

Sinônimo(s):

Agarose, cyclic carbonimidate, CNBr-Activated Agarose

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About This Item

Número CAS:
Número MDL:
Código UNSPSC:
41106500
NACRES:
NA.56

forma

lyophilized powder

técnica(s)

affinity chromatography: suitable

matriz

cross-linked 4% beaded agarose

Grupo ativo da matriz

cyanate or related structures

espaçador de matriz

1 atom (when ligands are coupled via isourea derivative or related linkage)

inchaço

1 g swells to 2.5-4.5 mL

capacidade

≥10 mg/mL binding capacity (BSA)(via amino groups)

adequação

suitable for chromatography

temperatura de armazenamento

−20°C

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Aplicação

Cyanogen bromide-activated Agarose is lyophilized powder stabilized with lactose used in affinity chromatography, protein chromatography, protein interactions, antibody labeling, antibody modification and attaching antibodies to agarose beads.

forma física

Lyophilized powder stabilized with lactose

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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C A Schall et al.
Biotechnology and bioengineering, 53(1), 41-48 (1997-01-05)
The stability of NAD(H) immobilized to a crosslinked agarose support (Sepharose(R)-4B) was examined in buffer solutions at a pH of 7.0 and 8.5. Specifically, this study investigated particle attrition and ligand leakage rates from a cyanogen bromide activated agarose support.
N A Morjana et al.
Protein expression and purification, 5(2), 144-148 (1994-04-01)
Protein disulfide isomerase (PDI) catalyzes the formation and rearrangement of disulfide bonds during protein folding. PDI coupled to cyanogen bromide-activated agarose retains its catalytic activity, and a column of this material increases both the rate and the yield for folding
R A Gilissen et al.
Biochemical pharmacology, 43(12), 2661-2663 (1992-06-23)
A method for the covalent binding of rat liver UDP-glucuronosyltransferase to a cyanogen bromide-activated agarose matrix is described. The rat liver microsomal fraction was solubilized with 8 mM 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate (CHAPS); 90% of the microsomal protein was solubilized. Some 50-60% of

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