Cell Signaling Technology

Product Pathways - Transcription Factors

FoxC1 (D8A6) Rabbit mAb #8758

Applications Reactivity Sensitivity MW (kDa) Isotype
W IP H M R Endogenous 75 Rabbit IgG

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

Protocols

Specificity / Sensitivity

FoxC1 (D8A6) Rabbit mAb recognizes endogenous levels of total FoxC1 protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the amino terminus of human FoxC1 protein.

Western Blotting

Western Blotting

Western blot analysis of extracts from various cell lines using FoxC1 (D8A6) Rabbit mAb.

Background

Forkhead box (Fox) proteins are a family of evolutionarily conserved transcription factors defined by the presence of a winged helix DNA binding domain called a Forkhead box (1). In humans, there are over 40 known Fox protein family members, divided into 19 subfamilies, which have evolved to regulate gene transcription in diverse and highly specialized biological contexts throughout development (2). Mutations that disrupt the expression of Fox gene family members have consequently been implicated in a broad array of human disorders, including immunological dysfunction, infertility, speech/language disorders, and cancer (3,4).

FoxC1 (FKHL7, FREAC3) is one of two mammalian FoxC subfamily members. Along with FoxC2, it is expressed in paraxial mesoderm where it functions to promote somitogenesis, myogenesis, and vascular development, possibly under Wnt/β-catenin regulation (5). Mutations in FoxC1 are implicated in anterior segment dysgenesis (ASD) disorders, including congenital glaucoma and Axenfeld-Rieger syndrome (6). Research studies have shown that alterations in FoxC1 expression are linked to breast cancer invasiveness (7,8) and have been shown to modulate proliferation and migration of breast cancer cells in vitro (9).

  1. Myatt, S.S. and Lam, E.W. (2007) Nat Rev Cancer 7, 847-59.
  2. Jackson, B.C. et al. (2010) Hum Genomics 4, 345-52.
  3. Hannenhalli, S. and Kaestner, K.H. (2009) Nat Rev Genet 10, 233-40.
  4. Benayoun, B.A. et al. (2011) Trends Genet, Epub ahead of print.
  5. Savage, J. et al. (2010) Differentiation 79, 31-40.
  6. Weisschuh, N. et al. (2008) Clin Genet 74, 476-80.
  7. Dejeux, E. et al. (2010) Mol Cancer 9, 68.
  8. Muggerud, A.A. et al. (2010) Breast Cancer Res 12, R3.
  9. Ray, P.S. et al. (2010) Cancer Res 70, 3870-6.

Application References

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Companion Products

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

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