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A6888

Sigma-Aldrich

Adenosine 5′-triphosphate–Agarose

aqueous glycerol suspension

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MDL number:
MFCD00801332
NACRES:
NA.56

form

aqueous glycerol suspension

Quality Level

200

extent of labeling

≥1 μmol per mL

matrix

cross-linked 4% beaded agarose

matrix activation

cyanogen bromide

matrix attachment

ribose hydroxyls

matrix spacer

11 atoms (adipic acid dihydrazide)

storage temp.

−20°C

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This Item
A1271G9768A2767
Sigma-Aldrich

Sigma-Aldrich

A6888

Adenosine 5′-triphosphate–Agarose

Adenosine 5′-monophosphate–Agarose lyophilized powder

Sigma-Aldrich

A1271

Adenosine 5′-monophosphate–Agarose

Guanosine 5′-triphosphate–Agarose aqueous glycerol suspension

Sigma-Aldrich

G9768

Guanosine 5′-triphosphate–Agarose

Adenosine 5′-triphosphate–Agarose lyophilized powder

Sigma-Aldrich

A2767

Adenosine 5′-triphosphate–Agarose

extent of labeling

≥1 μmol per mL

extent of labeling

1-5 μmol per mL

extent of labeling

1-5 μmol per mL

extent of labeling

1-5 μmol per mL

matrix

cross-linked 4% beaded agarose

matrix

cross-linked 4% beaded agarose

matrix

cross-linked 4% beaded agarose

matrix

cross-linked 4% beaded agarose

matrix activation

cyanogen bromide

matrix activation

cyanogen bromide

matrix activation

cyanogen bromide

matrix activation

cyanogen bromide

matrix attachment

ribose hydroxyls

matrix attachment

C-8

matrix attachment

ribose hydroxyls

matrix attachment

C-8

matrix spacer

11 atoms (adipic acid dihydrazide)

matrix spacer

9 atoms

matrix spacer

11 atoms (adipic acid dihydrazide)

matrix spacer

9 atoms

Application

Adenosine 5′-triphosphate Agarose (5′-ATP agarose) has been used in affinity chromatography to purify uridine kinase from Ehrlich ascites tumor cells.

Physical form

Suspension in 50% glycerol containing 0.25 M NaCl

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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PL860-CGA/SHF-1EA

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B Suri et al.
The EMBO journal, 3(3), 575-579 (1984-03-01)
The EcoA restriction enzyme from Escherichia coli 15T- has been isolated. It proves to be an unusual enzyme, clearly related functionally to the classical type I restriction enzymes. The basic enzyme is a two subunit modification methylase. Another protein species
E Scherzinger et al.
The Journal of biological chemistry, 272(48), 30228-30236 (1997-12-31)
The RepA protein of the mobilizable broad host range plasmid RSF1010 has a key function in its replication. RepA is one of the smallest known helicases. The protein forms a homohexamer of 29,896-Da subunits. A variety of methods were used
H D Kim et al.
Biochemistry, 38(44), 14697-14710 (1999-11-05)
Two polynucleotide-dependent ATPases, 95 and 181 kDa in size, have been purified to near homogeneity from cell-free extracts of Schizosaccharomyces pombe. Despite their size differences, their biochemical properties were strikingly similar. Both enzymes were capable of unwinding RNA and DNA
S Ogg et al.
The Journal of biological chemistry, 269(48), 30461-30469 (1994-12-02)
Human Cdc25C is a protein phosphatase that dephosphorylates and activates Cdc2-cyclin B to trigger entry into mitosis. Cdc25C is itself regulated by phosphorylation. In asynchronously growing HeLa cells, we have determined that serine 216 is the major site of Cdc25C
V Nagaraja et al.
Journal of molecular biology, 182(4), 579-587 (1985-04-20)
We have purified the type I restriction enzymes SB and SP from Salmonella typhimurium and S. potsdam, respectively, and determined the DNA sequences that they recognize. These sequences resemble those previously determined for the type I enzymes, EcoB, EcoK and
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