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C9024

Sigma-Aldrich

Cyanocorrin−Agarose

saline suspension

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About This Item

Numero MDL:
Codice UNSPSC:
23151817
NACRES:
NA.56

Stato

saline suspension

Grado di funzionalizzazione

0.3-0.5 mg per mL

Matrice

4% beaded agarose

Attivazione matrice

cyanogen bromide

Gruppi immobilizzati alla matrice

carboxyl

Braccio spaziatore

8 atoms

Capacità

1-3 mg/mL binding capacity (nonintrinsic factor (N 1883))

Temperatura di conservazione

2-8°C

Applicazioni

Cyanocorrin-agarose is an agarose conjugate in saline suspension used in affinity chromatography, protein chromatography and specialty resins. Cyanocorrin has been used in studies to determine electron densities of B12 vitamins.

Stato fisico

Suspension in 0.5 M NaCl containing preservative

Codice della classe di stoccaggio

12 - Non Combustible Liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Mamoru Yamanishi et al.
European journal of biochemistry, 269(18), 4484-4494 (2002-09-17)
Recombinant glycerol dehydratase of Klebsiella pneumoniae was purified to homogeneity. The subunit composition of the enzyme was most probably alpha 2 beta 2 gamma 2. When (R)- and (S)-propane-1,2-diols were used independently as substrates, the rate with the (R)-enantiomer was
Andrew D Lawrence et al.
The Journal of biological chemistry, 283(16), 10813-10821 (2008-02-12)
Vitamin B(12), the antipernicious anemia factor, is the cyano derivative of adenosylcobalamin, which is one of nature's most complex coenzymes. Adenosylcobalamin is made along one of two similar yet distinct metabolic pathways, which are referred to as the aerobic and
Stefan Mebs et al.
The journal of physical chemistry. A, 113(29), 8366-8378 (2009-07-03)
The electron densities of the three natural B(12)-vitamins, two of them being essential cofactors for animal life, were determined in a procedure combining high-order X-ray data collection at low to very low temperatures with high-level density functional calculations. In a
S M Frisbie et al.
Biochemistry, 32(50), 13886-13892 (1993-12-21)
The interactions of methylcobalamin with cobalophilin from human serum were analyzed using extended X-ray absorption fine structure (EXAFS) spectroscopy, photolysis of the cobalt-carbon bond of methylcobalamin, and a pKa determination of the protonation of the coordinated nitrogen of 5,6-dimethylbenzimidazole (DMB).

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