C9024
Cyanocorrin−Agarose
saline suspension
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About This Item
Formulario
saline suspension
Extensión del etiquetado
0.3-0.5 mg per mL
Matriz
4% beaded agarose
activación de la matriz
cyanogen bromide
unión a la matriz
carboxyl
espaciador de matriz
8 atoms
capacidad
1-3 mg/mL binding capacity (nonintrinsic factor (N 1883))
temp. de almacenamiento
2-8°C
Aplicación
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.
Forma física
Suspension in 0.5 M NaCl containing preservative
Código de clase de almacenamiento
12 - Non Combustible Liquids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
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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).
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
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
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