Cell Signaling Technology

Product Pathways - Metabolism

Phospho-AMPKβ1 (Ser108) Antibody #4181

AMP-activated-kinase   AMPK   beta-1 chain   p-ampk   pampk   PRKA   PRKAB   PRKAB1   PRKAB2  

No. Size Price
4181S 100 µl ( 10 western blots ) ¥3,900.00 现货查询 购买询价
4181T 20 µl ( 2 western blots ) ¥1,500.00 现货查询 购买询价
4181 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human,Mouse,Rat,Monkey, Endogenous 38 Rabbit
IP 1:50

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting, IP=Immunoprecipitation,

Specificity / Sensitivity

Phospho-AMPKβ1 (Ser108) Antibody detects endogenous levels of AMPKβ1 only when phosphorylated at serine 108. The antibody may cross-react with phosphorylated AMPKβ2 when phosphorylated at Ser109.

Phospho-AMPKβ1 (Ser108) Antibody用于检测内源性在108位丝氨酸残基磷酸化的AMPKβ1蛋白水平

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser108 of human AMPKβ1. Antibodies are purified by protein A and peptide affinity chromatography.

多克隆抗体通过用对应于人源AMPKβ1蛋白Ser108序列的合成肽免疫动物制备而得,抗体经蛋白A和肽段亲和层析纯化。

Western Blotting

Western Blotting

Western blot analysis of extracts from C2C12 cells, untreated (lanes 1,3) or oligomycin-treated (lanes 2,4), using Phospho-AMPKβ1 (Ser108) Antibody (upper) or AMPKβ1 Antibody #4182 (lower). Cell lysates were treated with λ phosphatase in lanes 3 and 4 to demonstrate the phospho-specificity of Phospho-AMPKβ1 (Ser108) Antibody.

Wetern blot检测C2C12细胞提取物,未处理(1,3)或用寡霉素(2,4)处理,所用抗体为Phospho-AMPKβ1 (Ser108) Antibody (上)和 AMPKβ1 Antibody #4182(下)。3,4道的细胞裂解液用λ 磷酸酶处理来显示磷酸化抗体的特异性

IP

IP

Immunoprecipitation of phosphorylated AMPKβ1 from untreated or oligomycin-treated C2C12 cells using Phospho-AMPKβ1 (Ser108) Antibody, followed by western blot analysis using the same antibody.

磷酸化AMPKβ1免疫沉淀,蛋白来源于未处理或用寡霉素处理的C2C12细胞的Western实验,所用抗体为Phospho-AMPKβ1 (Ser108) Antibody

Background

AMP-activated protein kinase (AMPK) is highly conserved from yeast to plants and animals and plays a key role in the regulation of energy homeostasis (1). AMPK is a heterotrimeric complex composed of a catalytic α subunit and regulatory β and γ subunits, each of which is encoded by two or three distinct genes (α1, 2; β1, 2; γ1, 2, 3) (2). The kinase is activated by an elevated AMP/ATP ratio due to cellular and environmental stress, such as heat shock, hypoxia, and ischemia (1). The tumor suppressor LKB1, in association with accessory proteins STRAD and MO25, phosphorylates AMPKα at Thr172 in the activation loop, and this phosphorylation is required for AMPK activation (3-5). AMPKα is also phosphorylated at Thr258 and Ser485 (for α1; Ser491 for α2). The upstream kinase and the biological significance of these phosphorylation events have yet to be elucidated (6). The β1 subunit is post-translationally modified by myristoylation and multi-site phosphorylation including Ser24/25, Ser96, Ser101, Ser108, and Ser182 (6,7). Phosphorylation at Ser108 of the β1 subunit seems to be required for the activation of AMPK enzyme, while phosphorylation at Ser24/25 and Ser182 affects AMPK localization (7). Several mutations in AMPKγ subunits have been identified, most of which are located in the putative AMP/ATP binding sites (CBS or Bateman domains). Mutations at these sites lead to reduction of AMPK activity and cause glycogen accumulation in heart or skeletal muscle (1,2). Accumulating evidence indicates that AMPK not only regulates the metabolism of fatty acids and glycogen, but also modulates protein synthesis and cell growth through EF2 and TSC2/mTOR pathways, as well as blood flow via eNOS/nNOS (1).

腺苷酸激活的蛋白激酶(AMPK)是一种在酵母,植物和动物界高度保守的蛋白激酶,它在能量平衡中发挥关键性的作用(1)。AMPK是异源三聚体复合物,由α催化亚基和β、γ两个调节亚基组成,每个亚基都由两到三个不同的基因编码(α1, 2; β1, 2; γ1, 2, 3)(2)。细胞或者环境因素的刺激,如热激,缺氧,缺血等,导致AMP/ATP浓度比的升高,AMP/ATP浓度比的升高可以激活AMPK。肿瘤抑制因子LKB1,与辅助蛋白STRAD和MO25相结合,在AMPK的α亚基活化环的172位苏氨酸上对其磷酸化,磷酸化对AMPK的激活是必需的(3-5)。AMPKα同样也可以在Thr258和Ser485(α1; α2是Ser491)位点磷酸化。此过程的上游激酶和这些位点磷酸化的生物学意义尚不明晰(6)。β1亚基有一些翻译后的修饰,包括豆蒄酰化修饰,以及在多个位点的磷酸化修饰(包括Ser24/25, Ser96, Ser101和Ser182)(6,7)。β1亚基Ser108的磷酸化可能对AMPK的激活来说是必需的,而Ser24/25和Ser182的磷酸化可能影响到AMPK的定位(7)。越来越多的证据表明,AMPK不仅调控机体的糖脂代谢,同时也通过EF2和TSC2/mTOR通路调控细胞生长和蛋白质的合成,以及通过eNOS/nNOS系统来调节血流量(1)。

  1. Hardie, D.G. (2004) J Cell Sci 117, 5479-87.
  2. Carling, D. (2004) Trends Biochem Sci 29, 18-24.
  3. Hawley, S.A. et al. (1996) J Biol Chem 271, 27879-87.
  4. Lizcano, J.M. et al. (2004) EMBO J 23, 833-43.
  5. Shaw, R.J. et al. (2004) Proc Natl Acad Sci USA 101, 3329-35.
  6. Woods, A. et al. (2003) J Biol Chem 278, 28434-42.
  7. Warden, S.M. et al. (2001) Biochem J 354, 275-83.

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