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Merck
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重要文件

C9024

Sigma-Aldrich

Cyanocorrin−Agarose

saline suspension

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About This Item

MDL號碼:
分類程式碼代碼:
23151817
NACRES:
NA.56

形狀

saline suspension

標籤範圍

0.3-0.5 mg per mL

基質

4% beaded agarose

基質活化

cyanogen bromide

基質結合

carboxyl

基質墊片

8 atoms

容量

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

儲存溫度

2-8°C

應用

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.

外觀

Suspension in 0.5 M NaCl containing preservative

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°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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