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Merck
CN
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14-770-M

Sigma-Aldrich

mTOR(1362端)蛋白,活性,10 µg

Active, N-terminal FLAG-tagged, recombinant, human mTOR, amino acids 1362-end, for use in Kinase Assays.

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别名:
FRAP1
UNSPSC代码:
12352200
eCl@ss:
32160405
NACRES:
NA.41

生物来源

human

质量水平

重组

expressed in baculovirus infected Sf21 cells

比活

377 U/mg

制造商/商品名称

Upstate®

技术

activity assay: suitable (kinase)

NCBI登记号

UniProt登记号

基因信息

human ... MTOR(2475)

一般描述

Research area: Cell Signaling

Protein Target: mTOR (FRAP1)

Target Sub-Family: Lipid/Atypical

N-terminal FLAG-tagged, recombinant, human mTOR, amino acids 1362-end

The mechanistic target of rapamycin (mTOR) protein is a serine/threonine protein kinase belonging to PI3K-related kinase (PIKK) family, expressed throughout the body.

应用

The active mTOR (1362-end) protein, 10 µg, has been used in the mTOR substrate phosphorylation assay to validate the biochemical and pharmacological profile of a novel mTOR-KI for targeting mTOR signaling pathways in vitro and in vivo.

生化/生理作用

Mechanistic target of rapamycin (mTOR) plays a pivotal role in regulating various essential cellular processes, ranging from protein synthesis to autophagy. Moreover, it influences metabolism, cellular survival, gene transcription, and cytoskeletal components. It gets activated in response to growth factors, nutrients, mitogens, and hormones.Downregulation of mTOR signaling is associated with the advancement of cancer and diabetes, and aging process.

包装

也有100 μg规格,请查询价格和供货情况。

单位定义

比活:其中一个单位的mTOR活性定义为在30°C下每分钟将1 nmole磷酸盐掺入2 mg/ml mTOR底物中,最终ATP浓度为100 µM。

外形

在100 µL 10mM HEPES、50mM NaCl、50 mMβ-甘油磷酸盐、0.25 mM原钒酸钠、10 mM NaF、300 µg/mL FLAGTM肽、20%v/v甘油中加入16 µg酶

储存及稳定性

储存在-70°C。 为了最大程度地回收产品,在取下盖子之前,将原始样品瓶进行离心。

法律信息

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

免责声明

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。

WGK

WGK 2


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Jianchang Qian et al.
Oncotarget, 7(41), 67071-67086 (2016-08-27)
The mechanistic target of rapamycin (mTOR) is a rational target for cancer treatment. While the mTORC1-selective rapalogs have shown significant benefits in the clinic, antitumor response may be further improved by inhibiting both mTORC1 and mTORC2. Herein, we established target
mTOR: Exploring a New Potential Therapeutic Target for Stroke
Castellanos M, et al.
Molecules to Medicine with mTOR, 105-122 (2016)
mTOR Signaling in Growth, Metabolism, and Disease
Saxton RA and Sabatini DM
Cells, 168(6), 960?976- 960?976 (2017)

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