Glucose / Energy Metabolism
AS160 (C69A7) Rabbit mAb
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| CSTコード |
包装 |
希望納入価格 (円) |
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| #2670S | 100 μL | 46,000 | |
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AS160抗体製品一覧
2670 の推奨プロトコール
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推奨プロトコールはCST社内試験の徹底的なバリデーションに基づいて作成されておりますので、正確かつ再現性の高い結果が得られます。
注:各製品に最適化されたプロトコールをリンクしています。
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2670:
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Immunoprecipitation
Western Blotting
| 用途(希釈倍率) | |
| ウエスタンブロッティング(1:1,000)、免疫沈降(1:50) |
| 特異性・感度 | |
| 内在性レベルのAS160 タンパク質を検出します。 |
| 使用抗原 | |
| ヒトのAS160 タンパク質のAla195 周辺領域(合成ペプチド) |
Western Blotting

Western blot analysis of extracts from HepG2, RD and 293T cells using AS160 (C69A7) Rabbit mAb.
The polypeptide insulin is a major hormone controlling critical energy functions such as glucose and lipid metabolism. Insulin binds to and activates the insulin receptor (IR) tyrosine kinase, which phosphorylates and recruits different adaptor proteins. The signaling pathway initiated by insulin and its receptor stimulates glucose uptake in muscle cells and adipocytes through translocation of GLUT4 glucose transporter from the cytoplasm to the plasma membrane (1). A 160 kDa substrate of the Akt Ser/Thr kinase (AS160, TBC1D4) is a Rab GTPase-activating protein that regulates insulin-stimulated GLUT4 trafficking. AS160 is expressed in many tissues including brain, kidney, liver, and brown and white fat (2). Multiple Akt phosphorylation sites have been identified on AS160 in vivo, with five sites (Ser318, Ser570, Ser588, Thr642, and Thr751) showing increased phosphorylation following insulin treatment (2,3). Studies using recombinant AS160 demonstrate that insulin-stimulated phosphorylation of AS160 is a crucial step in GLUT4 translocation (3) and is reduced in some patients with type 2 diabetes (4). The interaction of 14-3-3 regulatory proteins with AS160 phosphorylated at Thr642 is a necessary step for GLUT4 translocation (5). Phosphorylation of AS160 by AMPK is involved in the regulation of contraction-stimulated GLUT4 translocation (6).
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Watson, R.T. and Pessin, J.E. (2006) Trends Biochem. Sci. 31, 215-222.
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Kane, S. et al. (2002) J. Biol. Chem. 277, 22115-22118.
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Sano, H. et al. (2003) J. Biol. Chem. 278, 14599-14602.
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Karlsson, H.K. et al. (2005) Diabetes 54, 1692-1697.
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Ramm, G. et al. (2006) J. Biol. Chem. 281, 29174-29180.
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Kramer, H.F. et al. (2006) J. Biol. Chem. 281, 31478-31485.