Cell Signaling Technology

Product Pathways - Metabolism

Phospho-IRS-1 (Ser612) (L7B8) Mouse mAb #3193

insulin receptor substrate 1   insulin receptor substrate-1   insulin-receptor-substrate   IRS   IRS-1   IRS1   rtkscaffold  

No. Size Price
3193S 100 µl ( 10 western blots ) ¥3,900.00 现货查询 购买询价
3193 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human,Mouse,Rat, Endogenous 180 Mouse IgG2a

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting,

Specificity / Sensitivity

Phospho-IRS-1 (Ser612) (L7B8) Mouse mAb detects endogenous IRS-1 only when phosphorylated at serine 612.

Phospho-IRS-1 (Ser612) (L7B8)鼠单克隆抗体可识别内源性的Ser612磷酸化的IRS-1蛋白水平。

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser612 of mouse IRS-1.


Western Blotting

Western Blotting

Western blot analysis of extracts from differentiated C2C12 and CHO-IR/IRS-1 (CHO transfected with IR and IRS-1 cDNA) untreated or treated with insulin and λ phosphatase, using Phospho-IRS-1 (Ser612) (L7B8) Mouse mAb (upper), or IRS-1 Antibody #2382 (lower).

对分化的C2C12和CHO-IR/IRS-1细胞(用IR-IRS-1 cDNA转染CHO)(未处理,或胰岛素和λ磷酸酶处理),使用Phospho-IRS-1 (Ser612) (L7B8) Mouse mAb鼠单抗(上图)或IRS-1 Antibody #2382(下图)进行Western blot分析。


Insulin receptor substrate 1 (IRS-1) is one of the major substrates of the insulin receptor kinase (1). IRS-1 contains multiple tyrosine phosphorylation motifs that serve as docking sites for SH2-domain containing proteins that mediate the metabolic and growth-promoting functions of insulin (2-4). IRS-1 also contains over 30 potential serine/threonine phosphorylation sites. Ser307 of IRS-1 is phosphorylated by JNK (5) and IKK (6) while Ser789 is phosphorylated by SIK-2, a member of the AMPK family (7). The PKC and mTOR pathways mediate phosphorylation of IRS-1 at Ser612 and Ser636/639, respectively (8,9). Phosphorylation of IRS-1 at Ser1101 is mediated by PKCθ and results in an inhibition of insulin signaling in the cell, suggesting a potential mechanism for insulin resistance in some models of obesity (10).

胰岛素受体底物1(IRS-1)是胰岛素受体激酶的主要底物之一(1)。IRS-1包括多个酪氨酸磷酸化模体,作为与包含SH2结构域的蛋白质的接合位点,介导胰岛素的代谢和生长促进功能(2-4)。IRS-1也包含超过30个潜在的丝氨酸/苏氨酸磷酸化位点。JNK(5)和IKK(6)对IRS-1 Ser307位点进行磷酸化,SIK2(AMPK家族成员之一)对Ser789进行磷酸化(7)。PKC和mTOR途径分别介导IRS-1的Ser612和Ser636/639磷酸化(8,9)。IRS-1在Ser1101的磷酸化由PKCθ介导,可以导致细胞内胰岛素信号通路的抑制,这暗示其在某些肥胖模型中的胰岛素抵抗机制中发挥作用(10)。

  1. Sun, X.J. et al. (1991) Nature 352, 73-77.
  2. Sun, X.J. et al. (1992) J. Biol. Chem. 267, 22662-22672.
  3. Myers Jr., M.G. et al. (1993) Endocrinology 132, 1421-1430.
  4. Wang, L.M. et al. (1993) Science 261, 1591-1594.
  5. Rui, L. et al. (1997) J. Clin. Invest. 107, 181-189.
  6. Gao, Z. et al. (2002) J. Biol. Chem. 277, 48115-48121.
  7. Horike, N. et al. (2003) J. Biol. Chem. 278, 18440-18447.
  8. Ozes, O.N. et al. (2001) Proc. Natl. Acad. Sci. USA 98, 4640-4645.
  9. De Fea, K. and Ruth, R.A. (1997) Biochemistry 36, 12939-12947.
  10. Li, Y. et al. (2004) J. Biol. Chem. 279, 45304-45307.

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