Analysis Note
Routinely evaluated by using the phosphopeptide as a substrate for Alkaline Phosphatase in a non-radioactive malachite green based enzyme assay. The assay was performed using the Alkaline/Acid Phosphatase Assay Kit (R-R-A-pS-V-A), (17-128).
Biochem/physiol Actions
Protein Target: Alkaline Phosphatase
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Physical form
Lyophilized powder
Preparation Note
Lyophilized: Stable for 2 years at 4°C . Rehydrated: Stable for 1 year at -20°C.
Legal Information
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Dephosphorylation of phosphoproteins and synthetic phosphopeptides. Study of the specificity of the polycation-stimulated and MgATP-dependent phosphorylase phosphatases
Agostinis, P., et al
The Journal of Biological Chemistry, 262, 1060-1064 (1987)
Synthetic peptides as model substrates for the study of the specificity of the polycation-stimulated protein phosphatases.
Agostinis, P, et al.
European Journal of Biochemistry, 189, 235-241 (1990)
Further definition of the substrate specificity of the alpha-herpesvirus protein kinase and comparison with protein kinases A and C
Leader, D. P., et al
Biochimica et Biophysica Acta, 1091, 426-431 (1991)
Phosphorylated synthetic peptides as tools for studying protein phosphatases.
L A Pinna et al.
Biochimica et biophysica acta, 1222(3), 415-431 (1994-07-21)
K W Harder et al.
The Biochemical journal, 298 ( Pt 2), 395-401 (1994-03-01)
The intracellular domain of human protein tyrosine phosphatase beta (HPTP beta) (44 kDa) was expressed in bacteria, purified using epitope 'tagging' immunoaffinity chromatography, and characterized with respect to kinetic profile, substrate specificity and potential modulators of enzyme activity. A chromogenic
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