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Browse our FOXC1 (FOXC1) ELISA Kits

Full name:
Forkhead Box C1 ELISA Kits (FOXC1)
On www.antibodies-online.com are 21 Forkhead Box C1 (FOXC1) ELISA Kits from 6 different suppliers available. Additionally we are shipping FOXC1 Antibodies (91) 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 ELISA KIts Gene Name GeneID UniProt
FOXC1 2296 Q12948
FOXC1 17300 Q61572
FOXC1 364706  

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More ELISA Kits for FOXC1 Interaction Partners

Human Forkhead Box C1 (FOXC1) interaction partners

  1. FOXC1 is correlated with chemosensitivity to anthracycline and could be used as an indicator of chemosensitivity in sporadic triple-negative breast cancer

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

  3. 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.

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

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

  6. 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.

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

  8. 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.

  9. Disruptions of enhancers near FOXC1 and GMDS (show GMDS ELISA Kits) may influence brain development.

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

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

  1. Compound, NC-specific Foxc1; Foxc2 (show FOXC2 ELISA Kits) homozygous mutant mice have more severe defects in structures of the ocular surface, such as the cornea and eyelids, accompanied by significant declines in the expression of another key developmental factor, Pitx2 (show PITX2 ELISA Kits), and its downstream effector Dkk2 (show DKK2 ELISA Kits), which antagonizes canonical Wnt (show WNT2 ELISA Kits) signaling.

  2. 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.

  3. Foxc1 and Foxc2 (show FOXC2 ELISA Kits) maintain glomerular podocyte integrity by regulating the gene expression.

  4. Foxc1 and Foxc2 (show FOXC2 ELISA Kits) have a role in kidney and axial skeleton development.

  5. 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.

  6. deletion of Foxc1 and Foxc2 (show FOXC2 ELISA Kits) specifically in Pax3 (show PAX3 ELISA Kits)-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

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

  8. 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.

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

  10. 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

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

Protein level used designations for Forkhead Box C1 (FOXC1) ELISA Kits

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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