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Principaux documents

C9024

Sigma-Aldrich

Cyanocorrin−Agarose

saline suspension

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About This Item

Numéro MDL:
Code UNSPSC :
23151817
Nomenclature NACRES :
NA.56

Forme

saline suspension

Ampleur du marquage

0.3-0.5 mg per mL

Matrice

4% beaded agarose

Activation de la matrice

cyanogen bromide

Fixation de matrice

carboxyl

Espaceur de matrice

8 atoms

Capacité

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

Température de stockage

2-8°C

Application

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.

Forme physique

Suspension in 0.5 M NaCl containing preservative

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

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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