form
aqueous glycerol suspension
extent of labeling
1-3 μmol per mL
matrix
Cross-linked 4% beaded agarose
matrix activation
epoxy
matrix attachment
ribose hydroxyls
matrix spacer
22 atoms (adipic acid dihydrazide)
storage temp.
−20°C
Application
Uridine 5′-triphosphate-agarose (5′-UTP agarose) is used for protein chromatography, affinity chromatography, and nucleotide/coenzyme resins. Uridine 5′-triphosphate-agarose has been used to study uridine kinase from Ehrlich ascites carcinoma.
Physical form
Suspension in 50% glycerol containing 0.25 M NaCl and preservative
Disclaimer
For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.
存储类别
12 - Non Combustible Liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
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F Huang et al.
Biochemistry, 36(22), 6557-6563 (1997-06-03)
A selected RNA (isolate 6) efficiently catalyzes a self-capping reaction with free GDP, yielding the same 5'-capped structure as is formed by protein GTP:RNA guanylyltransferase. This unexplored RNA-catalyzed reaction type involving nucleophilic attack on phosphate by phosphate adds to the
Hani S Zaher et al.
RNA (New York, N.Y.), 12(11), 1949-1958 (2006-09-16)
We report the isolation and characterization of a second capping ribozyme, called 6.17. This ribozyme has substrate requirements that are very similar to a previously isolated capping ribozyme called Iso6. Both ribozymes promote capping and cap exchange reactions with a
C A van Eekelen et al.
The Journal of cell biology, 88(3), 554-563 (1981-03-01)
In this study, DNA-depleted nuclear protein matrices are isolated from HeLa S3 cells. These nuclear matrices consist of peripheral laminae, residual nucleoli, and internal fibrillar structures. High molecular weight, heterogeneous nuclear RNA (hnRNA) is quantitatively associated with these structures and
R C Payne et al.
The Journal of biological chemistry, 260(18), 10242-10247 (1985-08-25)
Uridine kinase from Ehrlich ascites tumor cells has been purified about 60,000-fold to apparent homogeneity and with an overall recovery of about 40%. This purification was achieved using phosphocellulose and adenosine 5'-triphosphate-agarose affinity chromatography. The subunit molecular mass as judged
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