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Transcript
Alkaline Phosphatase
(Escherichia coli)
Alkaline Phosphatase
(Escherichia coli)
Cat. No.
E1026-01
E1026-02
Size
30 units
150 units
Unit Definition:
One unit is the amount of
enzyme required to hydrolyze
1
µmol
of
pnitrophenylphosphate in 1 min
at 37oC in a buffer of 1 M
diethanolamine, 10 mM pnitrophenylphosphate, 0.25
mM MgCl2 (pH 9.8).
Storage Conditions:
Store at -20°C
Bacterial phosphatase catalyzes the hydrolysis of
phosphate esters, including those present in nucleic
acids and nucleotides.
Description:
> More thermal stable than Calf Intestine Alkaline
Phosphatase (CIAP, CIP).
> Optimal incubation temperature is approximately
60oC, however the enzyme remains active from
20oC to 80oC.
> Resistant to chemical changes and active over a
broad range of buffer conditions.
> Can be used to remove 5'-phosphates from DNA or
RNA prior to 5'-end labeling (1).
> Works to remove 5'-phosphates from linearized
vector molecules to prevent self-ligation of the
vector during cloning procedures (1).
> Ideal
for diagnostic immunoassays and
immunodetection of proteins and nucleic acids
following blotting experiments (1).
Storage Buffer:
20 mM Tris-HCl (pH 7.0 at 22oC), 5 mM potassium
phosphate, 100 mM KCl, 0.1 mM MgCl2, 0.1 mM ZnCl2 and
stabilizers.
Quality Control:
All preparations are assayed for contaminating
endonuclease and nonspecific RNase and single- and
double-stranded DNase activities.
References:
1. Sambrook, J. et al. (1989) Molecular cloning: A
laboratory Manual, second edition, pp. 1.56, 5.72 Cold
Spring Harbor, New York.
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