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Browse our anti-FOXC1 (FOXC1) Antibodies

Full name:
anti-Forkhead Box C1 Antibodies (FOXC1)
On www.antibodies-online.com are 91 Forkhead Box C1 (FOXC1) Antibodies from 14 different suppliers available. Additionally we are shipping FOXC1 Kits (21) and FOXC1 Proteins (5) and many more products for this protein. A total of 125 FOXC1 products are currently listed.
Synonyms:
ARA, CFKH-1, ch, fkh-1, Fkh1, FKHL7, foxc1, FREAC-3, FREAC3, frkhda, IGDA, IHG1, IRID1, Mf1, Mf4, RIEG3, xfd-11
list all antibodies Gene Name GeneID UniProt
FOXC1 2296 Q12948
FOXC1 17300 Q61572
FOXC1 364706  

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anti-Human FOXC1 Antibodies:

anti-Mouse (Murine) FOXC1 Antibodies:

anti-Rat (Rattus) FOXC1 Antibodies:

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Top referenced anti-FOXC1 Antibodies

  1. Human Polyclonal FOXC1 Primary Antibody for ChIP, ELISA - ABIN249940 : Dagenais, Hartsough, Erickson, Witte, Butler, Glover: Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome. in Gene expression patterns : GEP 2004 (PubMed)
    Show all 10 references for ABIN249940

  2. Human Polyclonal FOXC1 Primary Antibody for ChIP, EIA - ABIN374336 : Jelcick, Yuan, Leehy, Cox, Silveira, Qiu, Schenk, Sachs, Morrison, Nystuen, DeAngelis, Haider: Genetic variations strongly influence phenotypic outcome in the mouse retina. in PLoS ONE 2011 (PubMed)
    Show all 4 references for ABIN374336

  3. Human Polyclonal FOXC1 Primary Antibody for IHC, ELISA - ABIN185028 : Zhou, Kato, Asanoma, Kondo, Arima, Kato, Matsuda, Wake: Identification of FOXC1 as a TGF-beta1 responsive gene and its involvement in negative regulation of cell growth. in Genomics 2002 (PubMed)

  4. Human Polyclonal FOXC1 Primary Antibody for ELISA, WB - ABIN185525 : Berry, ONeill, Coca-Prados, Walter: FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated manner. in Molecular and cellular biology 2005 (PubMed)

  5. Human Polyclonal FOXC1 Primary Antibody for FACS, WB - ABIN652854 : Mears, Mirzayans, Gould, Pearce, Walter: Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25. in American journal of human genetics 1997 (PubMed)

  6. Human Polyclonal FOXC1 Primary Antibody for IHC, WB - ABIN2780363 : Berry, Skarie, Mirzayans, Fortin, Hudson, Raymond, Link, Walter: FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A. in Human molecular genetics 2008 (PubMed)

  7. Human Polyclonal FOXC1 Primary Antibody for WB - ABIN2779552 : Mortemousque, Amati-Bonneau, Couture, Graffan, Dubois, Colin, Bonneau, Morissette, Lacombe, Raymond: Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation family. in Archives of ophthalmology 2004 (PubMed)

More Antibodies against FOXC1 Interaction Partners

Human Forkhead Box C1 (FOXC1) interaction partners

  1. Elevated expression of FOXC1 enhanced the invasion ability of BLCB cells in vitro.

  2. this report describes an Italian family in which four subjects share brachydactyly type E and a 3 Mb microduplication in region 6p25. The duplication involves the gene FOXC1, expressed during the osteoblast differentiation, which appears a potential candidate gene for brachydactyly.

  3. miR (show MLXIP Antibodies)-495 acts as a tumour suppressor gene by targeting FOXC1 at the post-transcriptional level in endometrial cancer

  4. This report presents the clinical characteristics of a Belgian family with a 3.4 Mb deletion of chromosome 6p25, including the FOXC1 gene.

  5. data reveal the presence of translation regulatory sequences in the UTRs of FOXC1 and provide evidence for a possible role of rare FOXC1 variants as modifying factors of goniodysgenesis in primary congenital glaucoma.

  6. ARS (show SLURP1 Antibodies) is an autosomal dominant disorder with high penetration. It is primarily caused by a mutation of the pituitary homeobox 2 (PITX2 (show PITX2 Antibodies)) or forkhead box C1 (FOXC1) gene. Mutations in PITX2 (show PITX2 Antibodies) on chromosome 4q25, or in FOXC1 at 6p25, have been identified in approximately 40% to 70% of patients with ARS (show SLURP1 Antibodies)

  7. These data suggest that deregulation of FOXC1 or its downstream genes play a major role in the pathogenesis of coarctation of the aorta in humans.

  8. Disruptions of enhancers near FOXC1 and GMDS (show GMDS Antibodies) may influence brain development.

  9. We report a novel FOXC1 mutation (p. R127L) in a three-generation family with three ARS (show SLURP1 Antibodies) and heart defect (show Vcan Antibodies) patients.

  10. FOXC1 directly binds Gli2 (show GLI2 Antibodies) and potentiates Gli2 (show GLI2 Antibodies) DNA-binding activity.

Mouse (Murine) Forkhead Box C1 (FOXC1) interaction partners

  1. These findings offer the first evidence for a role of the meninges in brain vascular development and provide new insight into potential causes of cerebrovascular defects in patients with FOXC1 mutations.

  2. Foxc1 and Foxc2 (show FOXC2 Antibodies) maintain glomerular podocyte integrity by regulating the gene expression.

  3. Foxc1 and Foxc2 (show FOXC2 Antibodies) have a role in kidney and axial skeleton development.

  4. FOXC1 maintains the hair follicle stem cell niche and governs stem cell quiescence to preserve long-term tissue-regenerating potential.FOXC1 is necessary to establish a multiple-bulge hair follicle architecture.

  5. deletion of Foxc1 and Foxc2 (show FOXC2 Antibodies) specifically in Pax3 (show PAX3 Antibodies)-positive cells affects cell fate choices in the dermomyotome of somites at forelimb level, promoting the myogenic cell fate at the expense of endothelial cells that migrate to the limb

  6. Foxc1 is an important transcriptional partner of Ihh (show IHH Antibodies)-Gli2 (show GLI2 Antibodies) signalling during endochondral ossification, and that disruption of the Foxc1-Gli2 (show GLI2 Antibodies) interaction causes skeletal abnormalities observed in the Axenfeld-Rieger syndrome.

  7. In self-renewing stem cells (SCs), Foxc1 activates Nfatc1 and bone morphogenetic protein (BMP) signaling, two key mechanisms that govern quiescence. These findings reveal a dynamic, cell-intrinsic mechanism used by hair follicle SCs to reinforce quiescence upon self-renewal and suggest a unique ability of SCs to maintain cell identity.

  8. These observations reveal an essential role for Foxc1 in the early stage of vascular formation in the telencephalon.

  9. loss of Foxc1 non-autonomously induces a rapid and devastating decrease in embryonic cerebellar ventricular zone radial glial proliferation and concurrent increase in cerebellar neuronal differentiation

  10. A loss of Foxc1 function affects skull bone formation of the apical region.

FOXC1 Antigen Profile

Antigen Summary

This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined\; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.

Alternative names and synonyms associated with FOXC1

  • forkhead box C1 (foxc1) antibody
  • forkhead box C1 (FOXC1) antibody
  • Forkhead box protein C1 (foxc1) antibody
  • forkhead box C1 (Foxc1) antibody
  • forkhead box C1 (foxc1-b) antibody
  • ARA antibody
  • CFKH-1 antibody
  • ch antibody
  • fkh-1 antibody
  • Fkh1 antibody
  • FKHL7 antibody
  • foxc1 antibody
  • FREAC-3 antibody
  • FREAC3 antibody
  • frkhda antibody
  • IGDA antibody
  • IHG1 antibody
  • IRID1 antibody
  • Mf1 antibody
  • Mf4 antibody
  • RIEG3 antibody
  • xfd-11 antibody

Protein level used designations for anti-Forkhead Box C1 (FOXC1) Antibodies

forkhead box protein C1 , forkhead box C1 , Forkhead box protein C1 , forkhead, drosophila, homolog-like 7 , forkhead-related activator 3 , forkhead-related protein FKHL7 , forkhead-related transcription factor 3 , forkhead/winged helix-like transcription factor 7 , myeloid factor-delta , FREAC-3 , MF-1 , congenital hydrocephalus , mesoderm/mesenchyme forkhead 1 , transcription factor FKH-1 , forkhead box protein C1-B , winged helix protein CWH-6 , winged-helix transcription factor

GENE ID SPECIES
493250 Xenopus (Silurana) tropicalis
722918 Macaca mulatta
750577 Pan troglodytes
100028901 Monodelphis domestica
100195202 Salmo salar
2296 Homo sapiens
17300 Mus musculus
734912 Xenopus laevis
364706 Rattus norvegicus
395856 Gallus gallus
101102186 Ovis aries
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