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GJA8 encodes a transmembrane connexin protein that is necessary for lens growth and maturation of lens fiber cells. 再加上，我们可以发Gap Junction Protein, alpha 8, 50kDa 蛋白 (7)和数多这个蛋白质的别的产品。
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Human Polyclonal GJA8 Primary Antibody for WB - ABIN1882072
Shiels, Mackay, Ionides, Berry, Moore, Bhattacharya: A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q. in American journal of human genetics 1998
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Cow (Bovine) Polyclonal GJA8 Primary Antibody for ELISA - ABIN4264873
Lin, Liu, Lei, Fan, Liu, Yang, Wang, Liu, Yang: [A novel GJA8 mutation in a Chinese family with autosomal dominant congenital cataract]. in Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2008
These results suggest that expression of Cx50D47A induces ER stress, triggering activation of the PERK (显示 EIF2AK3 抗体)-ATF4 (显示 ATF4 抗体) pathway, which potentially contributes to the lens pathology and leads to increased expression of anti-apoptotic factors, allowing cell survival.
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
data show that expression and phosphorylation of Cx46 (显示 GJA3 抗体) and Cx50 are complementary in seminiferous tubules
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
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.
The Gja8(R205G) mutation differentially impairs the functions of Cx50 and Cx46 (显示 GJA3 抗体) to cause cataracts, small lenses and microphthalmia.
D3 residue plays an essential role in unitary conductance of Cx50 gap junction channels
Normal Cx50 function requires an intact PDZ domain (显示 INADL 抗体)-binding motif.
These results showed that the binding of calcium/calmodulin to the intracellular loop of connexin 50 (Cx50) is critical for mediating the Ca2 (显示 CA2 抗体)+-dependent inhibition of Cx50 gap junctions
Dense cataract and microphthalmia (dcm) in BALB/c mice is caused by mutations in the GJA8 gene.
GJA8 is the newly identified genetic cause of familial congenital cataract.
Data indicate de novo heterozygous mutations affecting the same codon of gap junction alpha-8 protein (GJA8) p.(Gly94Glu) and p.(Gly94Arg) )in 2 of the probands, in addition to the p.(Asp51Asn) mutation previously identified in the third case.
Study identified two novel missense mutations within P59 (显示 FKBP4 抗体) and R76 of Cx50 that are associated with autosomal dominant congenital cataracts (ADCC). Functional analysis showed that Cx50R76H localized at appositional membranes forming gap junctions with enormous cytoplasmic protein (显示 BLZF1 抗体) accumulation, whereas the Cx50P59A mutation was found inefficient at forming detectable plaques.
The novel insert mutation in the TM2 (显示 TPM2 抗体) domain of Cx50 protein, which impairs its trafficking to the cell membrane and gap-junction function, is associated with the cataract formation in this Chinese pedigree.
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
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.
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.
the role of the charged residues at the end of TM-1 in voltage sensing in Cx26 (显示 GJB2 抗体), Cx46 (显示 GJA3 抗体), and Cx50.
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 (显示 GJA3 抗体) and c.268 C > T in GJA3 (显示 GJA3 抗体)), one was previously reported (c.218 C > T in GJA8).
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.
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.
alpha 8 connexin
, 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