anti-FOXC1 (FOXC1) 抗体产品概述

Full name:
anti-Forkhead Box C1 抗体 (FOXC1)
在www.antibodies-online.cn可供92 Forkhead Box C1 (FOXC1) 抗体的14不同的供货商。 再加上,我们可以发FOXC1 试剂盒 (21)FOXC1 蛋白 (5)和数多这个蛋白质的别的产品。 总共126 FOXC1产品已列进来了。
别名:
ARA, CFKH-1, ch, fkh-1, Fkh1, FKHL7, foxc1, FREAC-3, FREAC3, frkhda, IGDA, IHG1, IRID1, Mf1, Mf4, RIEG3, xfd-11
列出全部抗体 基因 基因ID UniProt
FOXC1 2296 Q12948
FOXC1 17300 Q61572
FOXC1 364706  

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引用最多的anti-FOXC1 抗体

  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 249940

  2. 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)

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

  5. 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)

更多抗FOXC1的相互作用对抗体

Human Forkhead Box C1 (FOXC1) interaction partners

  1. Glaucoma prevalence and phenotype are characterized in a cohort of glaucoma patients and their family members with FOXC1 variants.

  2. FOXC1 and FOXC2 (显示 FOXC2 抗体) are essential regulators of lymphangiogenesis and may have roles in lymphatic-associated diseases

  3. This review will summarize current knowledge on the function and regulation of FOXC1 in tumor development and progression with a focus on basal-like breast cancer, as well as the implications of these new findings in cancer diagnosis and treatment. [review]

  4. Here, we demonstrate a novel FOXC1-driven mechanism that suppresses ERa expression in breast cancer. We find that FOXC1 competes with GATA-binding protein 3 (GATA3 (显示 GATA3 抗体)) for the same binding regions in the cis (显示 CISH 抗体)-regulatory elements upstream of the ERa gene and thereby downregulates ERa expression and consequently its transcriptional activity

  5. A novel heterozygous FOXC1 variant segregated with the disease in a family with Axenfeld Rieger Syndrome. A novel homozygous variant in the FOXC1 gene segregated in a family with ARS (显示 SLURP1 抗体) and congenital glaucoma.

  6. Our findings suggested that FOXCUT expression contributed to the development and progression of nasopharyngeal carcinoma by targeting FOXC1 and that FOXCUT might be useful as a potential nasopharyngeal carcinoma biomarker and therapeutic target.

  7. this study defines FOXC1 as a regulator specific for KC terminal differentiation and establishes its potential position in the genetic regulatory network.

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

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

  10. 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.

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

  1. FOXC1 and FOXC2 (显示 FOXC2 抗体) are essential regulators of lymphangiogenesis and may have roles in lymphatic-associated diseases

  2. These data indicate that Foxc1 expression is regulated by BMP4 (显示 BMP4 抗体) and FOXC1 functions in the commitment of progenitor cells to the osteoblast fate and its expression is reduced when differentiation proceeds.

  3. Foxc1 regulates sweat duct luminal cell differentiation and mimic apocrine miliaria.

  4. Compound, NC-specific Foxc1; Foxc2 (显示 FOXC2 抗体) 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 (显示 PITX2 抗体), and its downstream effector Dkk2 (显示 DKK2 抗体), which antagonizes canonical Wnt (显示 WNT2 抗体) signaling.

  5. 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.

  6. Foxc1 and Foxc2 (显示 FOXC2 抗体) maintain glomerular podocyte integrity by regulating the gene expression.

  7. Foxc1 and Foxc2 (显示 FOXC2 抗体) have a role in kidney and axial skeleton development.

  8. 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.

  9. deletion of Foxc1 and Foxc2 (显示 FOXC2 抗体) specifically in Pax3 (显示 PAX3 抗体)-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

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

FOXC1 抗原简介

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

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

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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