Cell Signaling Technology

Product Pathways - Lymphocyte Signaling

Itk (2F12) Mouse mAb #2380

Applications Reactivity Sensitivity MW (kDa) Isotype
W IP H (M) (R) (Mk) Endogenous 72 Mouse IgG1

Applications Key:  W=Western Blotting  IP=Immunoprecipitation
Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

Protocols

Specificity / Sensitivity

Itk (2F12) Mouse mAB detects endogenouse levels of total Itk protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with an amino-terminal peptide of Itk.

Western Blotting

Western Blotting

Western blot analysis of extracts from Jurkat, BaF3, THP-1, RAW and Raji cells, using Itk (2F12) Mouse mAb (upper) and beta-Actin Antibody (#4967) (lower).

Western Blotting

Western Blotting

Western blot analysis of extracts from Jurkat and HuT 78 cells, using Itk (2F12) Mouse mAb.

Background

Interleukin-2 inducible T-cell kinase (Itk, Emt or Tsk) is a member of the non-receptor protein tyrosine kinases. Family members of Itk include Tec, Btk, Rlk and Bmx and are all defined by a common structure: an amino-terminal PH domain, a Tec-homology domain and a SH3 and SH2 domain followed by a carboxy-terminal kinase domain (1). Tec, Rlk and Itk are expressed in T cells and activated in response to T cell receptor (TCR) engagement. Data demonstrate that Itk functions in signal transduction downstream of TCR and activates PLCgamma1 and Erk. Lck directly activates Itk through phosphorylation in the conserved activation loop at Tyr511, and furthermore, Itk is autophosphorylated in the SH3 domain at Tyr180. Itk-Y180F is still capable of phosphorylating PLCgamma1 in contrast to Itk-Y511F, which has lost that function (2-3). Itk -/- mice show reduced lung inflammation, eosinophil infiltration and mucous production in response to allergic asthma induction. Thus, Itk could become a desirable target for anti-asthmatic treatments (4).

  1. Schwartzberg, P.L. and Finkelstein, L.D. (2005) Nat Rev Immunol. 5, 284-295.
  2. Heyeck, S. D. et al. (1997) J Biol Chem. 272, 25401-25408.
  3. Wilcox, H.M. and Berg, L.J. (2003) J Biol Chem. 278, 37112-37121.
  4. Mueller, C. and August, A. (2003) J Immunol. 170, 5056-5063.

Application References

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For Research Use Only. Not For Use In Diagnostic Procedures.

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