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GJA4 Antibody

  • 中文名稱：
    GJA4兔多克隆抗體
  • 貨號：
    CSB-PA141320
  • 規(guī)格：
    ￥2024
  • 圖片：
    • Western blot analysis of extracts from Jurkat cells, using GJA4 antibody.
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品名稱：
    Rabbit anti-Homo sapiens (Human) GJA4 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    GJA4
  • 別名：
    GJA4; Gap junction alpha-4 protein; Connexin-37; Cx37
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human,Mouse
  • 免疫原：
    Synthesized peptide derived from nal of Human GJA4.
  • 免疫原種屬：
    Homo sapiens (Human)
  • 克隆類型：
    Polyclonal
  • 純化方式：
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 產(chǎn)品提供形式：
    Liquid
  • 應(yīng)用范圍：
    ELISA,WB
  • 推薦稀釋比：
    Application Recommended Dilution
    WB 1:500-1:3000
  • Protocols：
  • 儲存條件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期：
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

產(chǎn)品評價(jià)

靶點(diǎn)詳情

  • 功能：
    One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell.
  • 基因功能參考文獻(xiàn)：
    1. Data show that fluid shear stress activates NOTCH signaling, which upregulates GJA4 (commonly, Cx37) and downstream cell cycle inhibitor CDKN1B (p27). PMID: 29247167
    2. CONNEXIN-37 gene polymorphisms are an ischemic stroke risk factor in Northern Han Chinese. PMID: 29631604
    3. ur study describes for the first time an association of drug-resistant non-structural heart disease AF with the Cx37 1019C > T gene polymorphism. We also confirmed the association of the Cx40 - 26G > A polymorphism in patients with AF and structural disease. PMID: 29351227
    4. the present study reported on a Cx37 variant in two Caucasian primary ovarian insufficiency (POI)patients, which was absent in control Caucasian populations, and which had a deleterious effect in vitro. It is therefore suggested that in the genetic context of the Caucasian population, this variant may contribute to POI. PMID: 29207017
    5. This study shows that Cx37 C1019T and Cx40 A71G polymorphisms are not associated with cardioprotective role in Egyptians. PMID: 28969560
    6. The CX37 rs1764390 G allele is associated with increased susceptibility to sepsis, which may be involved in the process of sepsis via mediating the plasma levels of NO, IL-6 and CRP. PMID: 27939333
    7. The C allele in the CX37 gene might be associated with susceptibility to dilated cardiomyopathy (DCM) in Chinese Han; female carriers of the C allele had higher DCM risk compared with TT homozygotes than males PMID: 25501978
    8. The protective effect of the T allele of the Cx37 gene might be strongly modified by smoking; in women, this effect could be mediated through stem cells. PMID: 26588185
    9. Our findings suggest that the Cx37 C1019T variation may contribute to the risk of PCOS in the South Indian women. PMID: 26656196
    10. Review/Meta-analysis: Cx37 C1019T was a risk factor for myocardial infarction and a protective factor for coronary artery disease. PMID: 24937033
    11. The C allele in the CX37 gene might be associated with the susceptibility to EH in population of Wuxi, China. PMID: 24685073
    12. three variants in PNPLA3 gene may be a genetic risk factor for NASH PMID: 24773516
    13. the C1019T polymorphism may be a moderate risk factor for MI and that DM was likely a potential source of between-study heterogeneity. [META-ANALYSIS] PMID: 24333099
    14. Determination of Cx37 C1019T and eNOS G894T polymorphisms may be used to detect a genetic predisposition to the development of myocardial infarction in patients with hemodynamically insignificant atherosclerosis and in apparently healthy individuals. PMID: 24261225
    15. 1019C/T polymorphism in the CX37 gene is associated with susceptibility to coronary artery disease as well as restenosis after coronary stenting in male patients. PMID: 23926016
    16. It is suggested that the polymorphism in the Cx37 gene (but not Cx40 gene) potentially plays a significant role in the manifestation of AMI disease in Iranian population PMID: 23724624
    17. C1019T polymorphism in the connexin 37 gene is associated with Helicobacter pylori infection and gastric cancer. PMID: 22901223
    18. We report the presence of connexins in platelets, notably connexin37, and that the formation of gap junctions within platelet thrombi is required for the control of clot retraction. PMID: 22528526
    19. GJA4 polymorphism is not associated with stroke risk in the Taiwanese population. PMID: 22305353
    20. We propose that the establishment of gap junctional communication between Cx37-expressing platelets provides a mechanism to limit thrombus propensity. PMID: 21810657
    21. In women with higher fasting glycemia TT genotype of Cx37 polymorphism was protective against subclinical atherosclerosis. PMID: 21617605
    22. The gene for Cx37 was associated with subclinical atherosclerosis in women with type 1 and 2 diabetes and in women with advanced central obesity. PMID: 21208019
    23. Connexin 37 genetic variants significantly affect carotid IMT and contribute to future development of ischemic stroke PMID: 21044781
    24. Endothelium-dependent vasodilation is primarily mediated by connexin 37 in mesenteric artery. PMID: 21172909
    25. Cx37 C1019T polymorphism is associated with tumour cell proliferation. PMID: 20705954
    26. Data show for the first time a functional and specific interaction between eNOS and Cx37 in endothelial cells. PMID: 20081116
    27. These data suggest that alterations of specific connexins, in this case connexin 37, and resulting changes in intercellular communication may modulate endothelial cell growth and death. PMID: 15194487
    28. NO inhibits the intercellular transfer of small molecules by a specific influence on Cx37 PMID: 15481066
    29. Here, data for human connexin37 (hCx37) hemichannels indicate that voltage gating can be explained as block/unblock without the necessity for an independent voltage gate. PMID: 15504903
    30. T1019 Cx37 SNP has shown to be a risk factor for acute myocardial infarction (AMI). PMID: 15982495
    31. investigated whether the allelic variants 1019C and 1019T are differentially predictive of increased risk for coronary artery disease (CAD) and myocardial infarction (MI) PMID: 16677656
    32. The connexin37 C1019T polymorphism is not related with markers of subclinical atherosclerosis in young adults in Finland PMID: 17196598
    33. Cx37 is expressed in the vascular endothelium as well as in monocytes and macrophages and these three cell types are key players in atherogenesis. PMID: 17318613
    34. Connexin 37 is expressed in the granulosa layer of follicles in the human ovary, and expression of Cx37 in granulosa cells was not different between poor responder and nonpoor responder to ovulation induction. PMID: 17531234
    35. Study suggests that GJA4 gene C1019T polymorphism and/or its related C-C-D haplotype might contribute to an increased risk of CAD and potentially play an important role in the development of coronary atherosclerosis in northern Han Chinese. PMID: 18073482
    36. variation in the connexin gene may modify effects risk factors have on vascular function PMID: 18605953
    37. As much as half the length of the connexin N-terminus can be deleted without affecting formation of gap junction plaques, but an intact N-terminus is required for hemichannel gating and intercellular communication. PMID: 18664489
    38. The electrical properties of Cx37 hemichannels (HCs) and gap junction channels (GJCs) were measured with voltage-clamp methods. PMID: 19166859
    39. connexin37 C1019T polymorphism is associated with peripheral artery disease in Japanese type 2 diabetic patients. PMID: 19407064
    40. The alpha helical structure of the connexin 37 N terminus may be dispensable for protein localization, but it is required for channel and hemichannel function. PMID: 19478091

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  • 亞細(xì)胞定位：
    Cell membrane; Multi-pass membrane protein. Cell junction, gap junction.
  • 蛋白家族：
    Connexin family, Alpha-type (group II) subfamily
  • 組織特異性：
    Expressed in multiple organs and tissues, including heart, uterus, ovary, and blood vessel endothelium.
  • 數(shù)據(jù)庫鏈接：

    HGNC: 4278

    OMIM: 121012

    KEGG: hsa:2701

    STRING: 9606.ENSP00000343676

    UniGene: Hs.296310