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GJD2 encodes a member of the connexin protein family. 再加上，我们可以发Gap Junction Protein, delta 2, 36kDa 蛋白 (3)和数多这个蛋白质的别的产品。
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Human Polyclonal GJD2 Primary Antibody for IHC, IHC (fro) - ABIN4892179
Moore, Zhou, Sirois, Belinsky, Zecevic, Antic: Connexin hemichannels contribute to spontaneous electrical activity in the human fetal cortex. in Proceedings of the National Academy of Sciences of the United States of America 2014
Our studies have shown that the heritability of myopia makes 66.4% in Lithuania. We detected significant associations between the combinations of GJD2 CC and RASGRF1 (显示 RASGRF1 抗体) GT and odds ratio of developing myopia.
Study shows that human outer retina displays a diverse cohort of connexin 36 gap junctions that follows the general mammalian scheme and display a great functional diversity.
Sparse punctate Cx36 expression was seen in the myenteric plexus in nerve trunks and some platelet-derived growth factor receptor-alpha (显示 PDGFRA 抗体)-positive cell and interstitial cells of Cajal fibers in patients with Hirschsprung's disease.
Genetic variants in ZC3H11B, RSPO1, and GJD2 are associated with susceptibility to the development of high myopia in a Han Chinese population.
It was shown that the decreased level of the examined neuronal proteins was accompanied by the impaired coexpression of synaptophysin (显示 SYP 抗体)/neurofilaments and Cx36 in the series of astrocytomas--anaplastic astrocytomas--glioblastomas.
In this study, there was no association of the analyzed SNPs located in RASGRF1 (显示 RASGRF1 抗体). GJD2, and ACTC1 (显示 ACTC1 抗体) with pathological myopia.
Three SNP alleles in BRD2 (显示 BRD2 抗体), Cx-36, and ME2 (显示 CELSR1 抗体) and microdeletions in 15q13.3, 15q11.2, and 16p13.11 also contribute risk to juvenile myclonic epilepsy.
Cx36 GJs are highly cation-selective and should exhibit relatively low permeability to numerous vital negatively charged metabolites and high permeability to potassium ion, a major charge carrier in cell-cell communication.
A polymorphism of Cx36 gene is associated to certain forms of human diabetes
connexin genes Gjd2 coding for mCx36, Gjc1 (显示 GJC1 抗体) coding for mCx45 and Gja10 (显示 GJA9 抗体) coding for mCx57 in the mouse, a subset of 4 connexin genes, including the unique GJA9 (Cx59 (显示 GJA9 抗体)) and GJA10 (Cx62 (显示 GJa10 抗体)), could be detected at least as transcript isoforms in the human retina.
Interneuronal communication at gap junctions made by connexin 36 may not be regulated by direct phosphorylation of connexin 36, but possibly by phosphorylation of associated proteins.
Study suggests that Cx36 (GJD2) expression in the AII (显示 NLRP3 抗体)-mediated rod pathway is activity dependent in the developing rabbit retina
Results indicate that even though Cx36 may be required for electrical coupling of suprachiasmatic nucleus cells, it does not affect coupling of molecular clock gene rhythms. Thus, electrical coupling of neurons and coupling of circadian clock gene oscillations can be regulated independently in the suprachiasmatic nucleus.
In mice, strain differences were found, such that punctate labelling for Cx36 was differentially distributed in the molecular layer of C57BL/6 vs. CD1 (显示 CCND1 抗体) mice. Cx36-puncta were localized to processes of stellate cells and other cerebellar interneurons. The vast majority of Cx36-puncta co-localized with Cx45 (显示 GJC1 抗体)-puncta, which in turn was associated with the scaffolding protein zonula occludens-1 (显示 TJP1 抗体).
Cx36 deletion therefore disrupts normal regulation of sympathetic outflow with effects on cardiovascular parameters.
Deletion of connexin 36 increased the frequency and shifted the amplitude distributions of miniature inhibitory post synaptic potentials.
retinal aberrant activity was reduced in the rd10 (显示 PDE6B 抗体)/Cx36KO mice compared to rd10 (显示 PDE6B 抗体) controls, a direct evidence for involvement of Cx36-containing gap junctions in generating aberrant activity in RD.
The results suggest that electrical synapses formed by Cx36-containing gap junctions occur in most of the widely distributed centers of the auditory system.
The resilts of this study showed that the phosphorylation state of Cx36 as a key biochemical step at the crossroad of light-dark and circadian regulatory pathways that control photoreceptor coupling.
The magnitudes of the 2f1 (显示 KLRG1 抗体)-f2 distortion products were not different between Cx36 knockout and wild-type mice, suggesting similar cochlear function in the two groups
Mg(2 (显示 MCOLN1 抗体)+)-dependent synaptic plasticity of Cx36-containing electrical synapses could underlie neuronal circuit reconfiguration via changes in brain energy metabolism that affects neuronal levels of intracellular ATP and [Mg(2 (显示 MCOLN1 抗体)+)]i.
Gene expression data indicate that EPCs, or their soluble products, modulate the expression of the beta-cell surface molecule connexin 36 and affect glucose-stimulated insulin (显示 INS 抗体) release in vitro.
This gene encodes a member of the connexin protein family. Connexins are gap junction proteins which are arranged in groups of 6 around a central pore to form a connexon, a component of the gap junction intercellular channel. The channels formed by this protein allow cationic molecule exchange between human beta cells and may function in the regulation of insulin secretion.
, gap junction alpha-9 protein
, gap junction delta-2 protein
, connexin 35.1
, gap junction channel-forming protein
, gap junction membrane channel protein alpha 9
, gap junction protein, alpha 9, 36kDa
, gap junction protein, alpha 9, 59kDa
, gap junction protein, delta 2, 36kDa
, gap junction protein, alpha 9