Gap Junction Protein, alpha 8, 50kDa (GJA8) ELISA Kits

GJA8 encodes a transmembrane connexin protein that is necessary for lens growth and maturation of lens fiber cells. Additionally we are shipping Gap Junction Protein, alpha 8, 50kDa Antibodies (55) and Gap Junction Protein, alpha 8, 50kDa Proteins (7) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Mouse GJA8 GJA8 14616 P28236
Anti-Rat GJA8 GJA8 29601  
Anti-Human GJA8 GJA8 2703 P48165
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More ELISA Kits for Gap Junction Protein, alpha 8, 50kDa Interaction Partners

Mouse (Murine) Gap Junction Protein, alpha 8, 50kDa (GJA8) interaction partners

  1. These results suggest that expression of Cx50D47A induces ER stress, triggering activation of the PERK (show EIF2AK3 ELISA Kits)-ATF4 (show ATF4 ELISA Kits) pathway, which potentially contributes to the lens pathology and leads to increased expression of anti-apoptotic factors, allowing cell survival.

  2. Study showed that mouse horizontal cells establish a coupled dendritic network by Cx57 and two coupled axon terminal networks, one made of Cx50 and the other made of Cx57 channels

  3. data show that expression and phosphorylation of Cx46 (show GJA3 ELISA Kits) and Cx50 are complementary in seminiferous tubules

  4. demonstrate, at the whole gap junction channel level, a crucial role of the surface charge properties in the first transmembrane/first extracellular border domain in determining the efficiency of ion permeation and the Vj gating of Cx50

  5. Data show that Ca(V) 1.2 and 1.3 channels are expressed in lens, regulating phosphorylation of aquaporin-0 and myosin light chain and expression of connexins 50 and 46.

  6. The Gja8(R205G) mutation differentially impairs the functions of Cx50 and Cx46 (show GJA3 ELISA Kits) to cause cataracts, small lenses and microphthalmia.

  7. D3 residue plays an essential role in unitary conductance of Cx50 gap junction channels

  8. Norma (show INADL ELISA Kits)l Cx50 function require (show TJP1 ELISA Kits)s an intact PDZ domain-binding motif.

  9. These results showed that the binding of calcium/calmodulin to the intracellular loop of connexin 50 (Cx50) is critical for mediating the Ca2 (show CA2 ELISA Kits)+-dependent inhibition of Cx50 gap junctions

  10. Dense cataract and microphthalmia (dcm) in BALB/c mice is caused by mutations in the GJA8 gene.

Human Gap Junction Protein, alpha 8, 50kDa (GJA8) interaction partners

  1. study demonstrates that the mutant protein localized to the plasma membrane and formed functional intercellular channels. These data suggest that GJA8 c.658A>G is most likely a benign rare variant

  2. The missense mutation c.139G > A in GJA8 gene is associated with autosomal dominant congenital cataract in a six-generation Chinese family. The result of this present study provides further evidence that the p. D47N mutation in CX50 is a hot-spot mutation.

  3. The c.433G > T (p.G145W) mutation in the GJA8 gene was first reported to our best knowledge. The results of our study would further broaden the mutation spectrum of GJA8 associated with congenital cataract.

  4. the role of the charged residues at the end of TM-1 in voltage sensing in Cx26 (show GJB2 ELISA Kits), Cx46 (show GJA3 ELISA Kits), and Cx50.

  5. This study identified three mutations in three Chinese families with hereditary cataracts. Of the three mutations, two were novel (c.125 A > C in GJA3 (show GJA3 ELISA Kits) and c.268 C > T in GJA3 (show GJA3 ELISA Kits)), one was previously reported (c.218 C > T in GJA8).

  6. These results indicated that the mutant Cx50 (S276F) might inhibit the function of gap junction channel in a dominant negative manner, but inhibit the hemichannel function in a recessive negative manner.

  7. GJA8 mutation (p.V44A) is associated with autosomal dominant congenital cataract.

  8. This is a novel missense mutation [c.829C > T, (p.H277Y)] identified in exon 2 of Cx50.

  9. We have used trio-based exome sequencing to uncover a recurrent missense mutation in CRYGD (show CRYGD ELISA Kits) and two novel missense mutations in GJA8 associated with autosomal dominant cataract (show MIP ELISA Kits) in three nuclear families.

  10. Tthe molecular consequences of the p.P88T mutation in GJA8 include changes in connexin 50 protein localization patterns.

Gap Junction Protein, alpha 8, 50kDa (GJA8) Antigen Profile

Antigen Summary

This gene encodes a transmembrane connexin protein that is necessary for lens growth and maturation of lens fiber cells. The encoded protein is a component of gap junction channels and functions in a calcium and pH-dependent manner. Mutations in this gene have been associated with zonular pulverulent cataracts, nuclear progressive cataracts, and cataract-microcornea syndrome.

Gene names and symbols associated with GJA8

  • gap junction protein, alpha 8 (Gja8) antibody
  • gap junction protein alpha 8 (GJA8) antibody
  • Aey5 antibody
  • CAE antibody
  • CAE1 antibody
  • Cnx50 antibody
  • CTRCT1 antibody
  • Cx45.6 antibody
  • CX50 antibody
  • CZP1 antibody
  • Lop10 antibody
  • MP70 antibody

Protein level used designations for GJA8

alpha 8 connexin , connexin-50 , gap junction alpha-8 protein , gap junction membrane channel protein alpha 8 , lens fiber protein MP70 , lens opacity 10 , connexin 50 , cell surface glycoprotein , gap junction membrane channel protein alpha-8 , lens intrinsic membrane protein MP70 , connexin 45.6 , connexin-45.6 , MP38 , MP64 , connexin-49 , cx49

14616 Mus musculus
29601 Rattus norvegicus
2703 Homo sapiens
395846 Gallus gallus
100170231 Ovis aries
483156 Canis lupus familiaris
524042 Bos taurus
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