Browse our anti-Ectodysplasin A (EDA) Antibodies

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anti-Ectodysplasin A Antibodies (EDA)
On www.antibodies-online.com are 105 Ectodysplasin A (EDA) Antibodies from 20 different suppliers available. Additionally we are shipping Ectodysplasin A Proteins (14) and Ectodysplasin A Kits (12) and many more products for this protein. A total of 138 Ectodysplasin A products are currently listed.
Synonyms:
0610040D20Rik, 2900052N06Rik, c11orf5, ECTD1, ED1, ED1-A1, ED1-A2, Eda-A1, Eda-A2, EDA1, EDA2, HED, HED1, mED1, ODT1, RGD1563178, si:ch73-223d24.5, STHAGX1, Ta, tabby, XHED, XLHED
list all antibodies Gene Name GeneID UniProt
EDA 66070 Q9JHS9
EDA 1896 Q92838
EDA 302424  

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anti-Mouse (Murine) Ectodysplasin A Antibodies:

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anti-Rat (Rattus) Ectodysplasin A Antibodies:

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Top referenced anti-Ectodysplasin A Antibodies

  1. Cow (Bovine) Polyclonal Ectodysplasin A Primary Antibody for WB - ABIN2781905 : Zhao, Watt, Battle, Li, Bondow, Duncan: Loss of both GATA4 and GATA6 blocks cardiac myocyte differentiation and results in acardia in mice. in Developmental biology 2008 (PubMed)
    Show all 2 references for 2781905

  2. Human Polyclonal Ectodysplasin A Primary Antibody for IHC, ELISA - ABIN1584385 : Li, Yao, Sheng, Yang, Ma: Dual-modal tracking of transplanted mesenchymal stem cells after myocardial infarction. in International journal of nanomedicine 2011 (PubMed)
    Show all 2 references for 1584385

  3. Human Polyclonal Ectodysplasin A Primary Antibody for EIA, IHC (p) - ABIN358789 : Tariq, Wasif, Ayub, Ahmad: A novel 4-bp insertion mutation in EDA1 gene in a Pakistani family with X-linked hypohidrotic ectodermal dysplasia. in European journal of dermatology : EJD 2007 (PubMed)
    Show all 2 references for 358789

  4. Cow (Bovine) Polyclonal Ectodysplasin A Primary Antibody for WB - ABIN2773846 : Zhao, Hua, Zhao, Meng, Ao, Liu, Shang, Sun, Lo, Zhang: Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia. in The British journal of dermatology 2008 (PubMed)
    Show all 2 references for 2773846

  5. Human Polyclonal Ectodysplasin A Primary Antibody for IF (p), IHC (p) - ABIN738381 : Oya, Yokoyama, Kokuryo, Uno, Yamauchi, Nagino: Inhibition of Toll-like receptor 4 suppresses liver injury induced by biliary obstruction and subsequent intraportal lipopolysaccharide injection. in American journal of physiology. Gastrointestinal and liver physiology 2014 (PubMed)

  6. Human Polyclonal Ectodysplasin A Primary Antibody for FACS, IF (p) - ABIN1713994 : Sisto, Barca, Lofrumento, Lisi: Downstream activation of NF-κB in the EDA-A1/EDAR signalling in Sjögren's syndrome and its regulation by the ubiquitin-editing enzyme A20. in Clinical and experimental immunology 2016 (PubMed)

More Antibodies against Ectodysplasin A Interaction Partners

Mouse (Murine) Ectodysplasin A (EDA) interaction partners

  1. Murine nasal submucosal glands express EDA during embryonic development. EDA signalling is essential for Lateral Nasal Gland and Medial Nasal Gland budding and ductal morphogenesis.

  2. Mouse models with HED also carry Eda, Edar (show EDAR Antibodies) or Edaradd (show EDARADD Antibodies) mutations and have defects that map to the same structures.We report that otitis media, rhinitis and nasopharyngitis occur at high frequency in Eda and Edar (show EDAR Antibodies) mutant mice and explore the pathogenic mechanisms related to glandular function, microbial and immune parameters in these lines

  3. Wnt (show WNT2 Antibodies), Eda, and Shh (show SHH Antibodies) have roles in touch dome Merkel cell development

  4. Using an ex vivo culture system, we show that suppression of canonical Wnt (show WNT2 Antibodies) signalling leads to a dose-dependent inhibition of supernumerary placodes in K14 (show KRT14 Antibodies)-Eda tissue explants.

  5. Eda and activin A (show INHBA Antibodies) are upstream regulators of Foxi3 (show FOXI3 Antibodies) in skin appendage placodes

  6. Ectodysplasin regulates activator-inhibitor balance in murine tooth development through Fgf20 (show FGF20 Antibodies) signaling.

  7. NF-kappaB (show NFKB1 Antibodies) downstream of the TNF (show TNF Antibodies)-like ligand ectodysplasin (Eda) is identified as a unique regulator of embryonic and prepubertal ductal morphogenesis.

  8. Data found that Eda regulates growth and branching of the SMG (show SNRPG Antibodies) via transcription factor NF-kappaB (show NFKB1 Antibodies) in the epithelium, and that the hedgehog (show SHH Antibodies) pathway is an important mediator of Eda/NF-kappaB (show NFKB1 Antibodies).

  9. Dkk4 (show DKK4 Antibodies) affects an auxiliary pathway for Eda-independent development of secondary hair

  10. Treatment of Eda-/- minor salivary gland explants with EDA A1 rescues minor salivary gland induction.

Human Ectodysplasin A (EDA) interaction partners

  1. EDA is an important candidate gene for two developmental diseases sharing the common feature of the congenital lack of teeth. In addition, these results can support the hypothesis that X-linked HED and EDA-related NTA are the same disease with different degrees of severity.

  2. EDA-A2 and its receptor XEDAR (show EDA2R Antibodies) are overexpressed in epithelial cells of salivary glands in Sjogren's syndrome patients, in comparison with healthy individuals. The EDA-A2/XEDAR (show EDA2R Antibodies) system in these cells is involved in the induction of apoptosis via CASP3 (show CASP3 Antibodies) activation.

  3. Based on a computerized protein structure analysis, we suggest that the change p.Arg289His in EDA impairs protein stabilization and thus might possibly be involved in the development of oligodontia concomitant with a mild ED phenotype.

  4. we identified a novel and three reported EDA missense mutations in four of six patients with X-linked hypohidrotic ectodermal dysplasia. Missense mutations and the mutations affecting the tumor necrosis factor (show TNF Antibodies) homology domain were correlated with fewer missing teeth.

  5. Our findings indicate that a novel mutation (c.878T>G) of EDA is associated with XLHED and adds to the repertoire of EDA mutations.

  6. We found a novel missense mutation in exon 1 of the EDA1 gene in a putative Mayan family from Mexico with XL-HED.

  7. A novel missense mutation in the EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia.

  8. dentified a novel deletion mutation located in exon 1 which if expressed would produce a highly truncated protein in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia

  9. novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesis

  10. novel one-nucleotide deletion mutation (c.855delG) of EDA in exon 8 which caused premature termination of the polypeptide at amino acid 307 was confirmed

Cow (Bovine) Ectodysplasin A (EDA) interaction partners

  1. Authors identifya mutation, never described before, that changes the regulation of alternative splicing in the EDA gene and causes ectodermal dysplasia in cattle.

  2. The 161-bp-long LINE1-derived-pseudoexon introduces a shift in reading frame and a premature stop codon early in EDA exon 2 and is probably the cause of XHED in this Danish Red Holstein family.

  3. describe a novel mutation of the EDA gene in which a 19 bp deletion in exon 1 in male Holstein calves demonstrated the phenotypic features of EDA

Zebrafish Ectodysplasin A (EDA) interaction partners

  1. Eda and edar (show EDAR Antibodies) are not required for early development but are specific for the development of adult skeletal and dental structures.

Ectodysplasin A (EDA) Antigen Profile

Antigen Summary

The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene.

Alternative names and synonyms associated with Ectodysplasin A (EDA)

  • ectodysplasin A (EDA) antibody
  • CWC15 homolog (S. cerevisiae) (Cwc15) antibody
  • ectodysplasin A (eda) antibody
  • ectodysplasin-A (Eda) antibody
  • 0610040D20Rik antibody
  • 2900052N06Rik antibody
  • c11orf5 antibody
  • ECTD1 antibody
  • ED1 antibody
  • ED1-A1 antibody
  • ED1-A2 antibody
  • Eda-A1 antibody
  • Eda-A2 antibody
  • EDA1 antibody
  • EDA2 antibody
  • HED antibody
  • HED1 antibody
  • mED1 antibody
  • ODT1 antibody
  • RGD1563178 antibody
  • si:ch73-223d24.5 antibody
  • STHAGX1 antibody
  • Ta antibody
  • tabby antibody
  • XHED antibody
  • XLHED antibody

Protein level used designations for anti-Ectodysplasin A (EDA) Antibodies

ectodysplasin A , embryonic development factor 1 , nucleoporin , protein CWC15 homolog , spliceosome-associated protein CWC15 homolog , X-linked anhidroitic ectodermal dysplasia protein , ectodysplasin-A , oligodontia 1 , ectodysplasin A1 , ectodermal dysplasia 1, anhidrotic , ectodermal dysplasia protein , ectodysplasin-1 , nackt , nkt , EDA protein homolog

GENE ID SPECIES
473652 Pan troglodytes
66070 Mus musculus
1896 Homo sapiens
769069 Gallus gallus
491935 Canis lupus familiaris
616179 Bos taurus
798740 Danio rerio
13607 Mus musculus
302424 Rattus norvegicus
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