产品名称
苏氨酸磷酸肽（K-R-pT-I-R-R）,
manufacturer/tradename
Upstate®
technique(s)
activity assay: suitable (kinase)
shipped in
wet ice
Quality Level
Analysis Note
通过使用PP2A免疫沉淀磷酸酶测定试剂盒（17-313）将该磷酸肽用作PP2A（14-111）的底物进行常规评估。 也可以使用Ser/Thr磷酸酶测定试剂盒1（17-127）进行测试。
Biochem/physiol Actions
蛋白质靶标：PP2A
Disclaimer
除非我们的产品目录或产品附带的其他公司文档另有说明，否则我们的产品仅供研究使用，不得用于任何其他目的，包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
Physical form
冻干粉末
Preparation Note
冻干：在4°C下可稳定保存2年。再水化：在-20°C下可稳定保存1年。
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
P Agostinis et al.
European journal of biochemistry, 205(1), 241-248 (1992-04-01)
p34cdc2 kinase, a critical regulator of the cell cycle, has been shown to recognize the consensus sequence S/TP in proteins such as histone H1, the retinoblastoma gene product RB and the carboxyl-terminal domain of eukaryotic RNA polymerase II. Using phosphorylated
M F Santoro et al.
The Journal of biological chemistry, 273(21), 13119-13128 (1998-05-28)
Although the available evidence suggests that whereas the caspase family plays a major role in apoptosis, they are not the sole stimulators of death. A random yeast two-hybrid screen of a lymphocyte cDNA library (using caspase-3 as the bait) found
A Donella-Deana et al.
Biochimica et biophysica acta, 1094(1), 130-133 (1991-08-13)
The four main classes of protein phosphatases (PP-1, 2A, 2B and 2C), although differing in their ability to dephosphorylate phosphopeptide substrates, invariably display a marked preference toward phosphothreonyl peptides over their phosphoseryl counterparts. Conversely, all the acidic and alkaline phosphatases
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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