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Merck
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文件

07-681

Sigma-Aldrich

抗磷酸化AMPK α(Thr172) 抗体

Upstate®, from rabbit

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物源

rabbit

品質等級

抗體表格

purified immunoglobulin

抗體產品種類

primary antibodies

無性繁殖

polyclonal

物種活性

human, rat

製造商/商標名

Upstate®

技術

western blot: suitable

同型

IgG

UniProt登錄號

運輸包裝

wet ice

目標翻譯後修改

phosphorylation (pThr172)

基因資訊

human ... PRKAA1(5562)

特異性

可识别磷酸化AMPKα。

免疫原

KLH偶联的合成肽,对应于人AMP活化蛋白激酶α2(AMPKα2)的磷酸化Thr172周围的氨基酸。

應用

抗磷酸化AMPK α(Tyr342)抗体是针对磷酸化AMPKα(Tyr342)的抗体,可用于WB。

品質

已通过免疫印迹对过夜饥饿的HEK293 细胞和部分纯化的大鼠肝脏AMPK的RIPA裂解液进行了常规评估

標靶描述

Mr 63 kDa

外觀

形式:纯化

分析報告

对照
血清饥饿HEK293 细胞

其他說明

浓度:请参考批次特异性浓缩物的检验报告。

法律資訊

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

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1


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B E Kemp et al.
Biochemical Society transactions, 31(Pt 1), 162-168 (2003-01-28)
The AMP-activated protein kinase (AMPK) is a metabolic-stress-sensing protein kinase that regulates metabolism in response to energy demand and supply by directly phosphorylating rate-limiting enzymes in metabolic pathways as well as controlling gene expression.
Enhanced external counterpulsation improves peripheral artery function and glucose tolerance in subjects with abnormal glucose tolerance.
Martin, JS; Beck, DT; Aranda, JM; Braith, RW
Journal of Applied Physiology (1985)
Tue L Nielsen et al.
Molecular genetics and metabolism, 123(1), 21-27 (2017-11-28)
McArdle disease (glycogen storage disease type V) is an inborn error of skeletal muscle metabolism, which affects glycogen phosphorylase (myophosphorylase) activity leading to an inability to break down glycogen. Patients with McArdle disease are exercise intolerant, as muscle glycogen-derived glucose
Roles of 5'-AMP-activated protein kinase (AMPK) in mammalian glucose homoeostasis.
Rutter, Guy A, et al.
The Biochemical Journal, 375, 1-16 (2003)
J F P Wojtaszewski et al.
Biochemical Society transactions, 31(Pt 6), 1290-1294 (2003-12-04)
The AMPK (5'AMP-activated protein kinase) is becoming recognized as a critical regulator of energy metabolism. However, many of these effects in muscle metabolism have been ascribed to AMPK based on the use of the unspecific activator AICAR (5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside). Using mouse

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