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Merck
CN
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14-334-M

Sigma-Aldrich

PRAK Protein, active, 15 µg

Active, N-terminal His6-tagged recombinant, human, full-length PRAK, for use in Kinase Assays.

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UNSPSC代码:
12352202
eCl@ss:
32160405
NACRES:
NA.32

生物来源

human

质量水平

100
300

重组

expressed in baculovirus infected Sf21 cells

分子量

Mw 55 kDa

制造商/商品名称

Upstate®

技术

activity assay: suitable (kinase)

UniProt登记号

一般描述

N-terminal His6-tagged recombinant, human, full-length PRAK
Product Source: expressed by baculovirus in Sf21 insect cells

生化/生理作用

Protein Target: PRAK
Target Sub-Family: CAMK

包装

Also available in 250μg size (2x125μg) - Call for pricing and availability. Please reference catalog number 14-334M when ordering the 250μg size.

质量

routinely evaluated by phosphorylation of PRAK Substrate Peptide

外形

Ni2+/NTA-agarose

储存及稳定性

6 months at -70C

其他说明

For Specific Activity data, refer to the Certificate of Analysis for individual lots of this enzyme.

法律信息

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

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.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Sens. 1

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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L New et al.
The EMBO journal, 17(12), 3372-3384 (1998-06-17)
We have identified and cloned a novel serine/ threonine kinase, p38-regulated/activated protein kinase (PRAK). PRAK is a 471 amino acid protein with 20-30% sequence identity to the known MAP kinase-regulated protein kinases RSK1/2/3, MNK1/2 and MAPKAP-K2/3. PRAK was found to
S P Davies et al.
The Biochemical journal, 351(Pt 1), 95-105 (2000-09-22)
The specificities of 28 commercially available compounds reported to be relatively selective inhibitors of particular serine/threonine-specific protein kinases have been examined against a large panel of protein kinases. The compounds KT 5720, Rottlerin and quercetin were found to inhibit many

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