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GJA8 Antibody

  • 货号：
    CSB-PA009449LA01HU
  • 规格：
    ￥440
  • 促销：
    小规格抗体限时一口价
  • 图片：
    • Western Blot
      Positive WB detected in: Hela whole cell lysate, A549 whole cell lysate, Rat brain tissue, Mouse brain tissue
      All lanes: GJA8 antibody at 2.5μg/ml
      Secondary
      Goat polyclonal to rabbit IgG at 1/50000 dilution
      Predicted band size: 49 kDa
      Observed band size: 49 kDa
    • Immunohistochemistry of paraffin-embedded human liver cancer using CSB-PA009449LA01HU at dilution of 1:100
    • Immunohistochemistry of paraffin-embedded human breast cancer using CSB-PA009449LA01HU at dilution of 1:100
    • Immunofluorescent analysis of HepG2 cells using CSB-PA009449LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
  • 其他：

产品详情

  • 产品名称：
    Rabbit anti-Homo sapiens (Human) GJA8 Polyclonal antibody
  • Uniprot No.：
    P48165
  • 基因名：
    GJA8
  • 别名：
    GJA8; Gap junction alpha-8 protein; Connexin-50; Cx50; Lens fiber protein MP70
  • 宿主：
    Rabbit
  • 反应种属：
    Human, Mouse, Rat
  • 免疫原：
    Recombinant Human Gap junction alpha-8 protein (286-432AA)
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    Non-conjugated

    本页面中的产品，GJA8 Antibody (CSB-PA009449LA01HU)，的标记方式是Non-conjugated。对于GJA8 Antibody，我们还提供其他标记。见下表：

    可提供标记
    标记方式 货号 产品名称 应用
    HRP CSB-PA009449LB01HU GJA8 Antibody, HRP conjugated ELISA
    FITC CSB-PA009449LC01HU GJA8 Antibody, FITC conjugated
    Biotin CSB-PA009449LD01HU GJA8 Antibody, Biotin conjugated ELISA
  • 克隆类型：
    Polyclonal
  • 抗体亚型：
    IgG
  • 纯化方式：
    >95%, Protein G purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA, WB, IHC, IF
  • 推荐稀释比：
    Application Recommended Dilution
    WB 1:500-1:5000
    IHC 1:20-1:200
    IF 1:50-1:200
  • Protocols：
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    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.

产品评价

靶点详情

  • 功能：
    Structural component of eye lens gap junctions. Gap junctions are dodecameric channels that connect the cytoplasm of adjoining cells. They are formed by the docking of two hexameric hemichannels, one from each cell membrane. Small molecules and ions diffuse from one cell to a neighboring cell via the central pore.
  • 基因功能参考文献：
    1. this study identified the genetic susceptibility of GJA8 polymorphisms on ARC and provides new clues for fully understanding the pathological mechanism of GJA8 variants in affecting lens opacity PMID: 30349978
    2. The mutation c.139G>A in the GJA8 gene detected in the present study was also previously reported in Caucasian and Chinese families but with different phenotypes, i.e. nuclear and nuclear pulverulent cataracts. Thus, the mutation c.139G>A in GJA8 appears to exhibit marked interfamilial phenotypic variability. PMID: 30262699
    3. The p.V44M mutation in the GJA8 gene was the most common mutation and was due to a founder effect within the Chinese congenital cataract cohort studied. PMID: 30078984
    4. GJA8 is the newly identified genetic cause of familial congenital cataract. PMID: 29434075
    5. 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. PMID: 28455998
    6. Study identified two novel missense mutations within P59 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 accumulation, whereas the Cx50P59A mutation was found inefficient at forming detectable plaques. PMID: 27216975
    7. The novel insert mutation in the TM2 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. PMID: 29489419
    8. 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 PMID: 28827829
    9. 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. PMID: 28526010
    10. 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. PMID: 27785597
    11. 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. PMID: 26174669
    12. GJA8 mutation (p.V44A) is associated with autosomal dominant congenital cataract. PMID: 25517998
    13. This is a novel missense mutation [c.829C > T, (p.H277Y)] identified in exon 2 of Cx50. PMID: 25947639
    14. We have used trio-based exome sequencing to uncover a recurrent missense mutation in CRYGD and two novel missense mutations in GJA8 associated with autosomal dominant cataract in three nuclear families. PMID: 25403472
    15. Tthe molecular consequences of the p.P88T mutation in GJA8 include changes in connexin 50 protein localization patterns. PMID: 24535056
    16. A recurrent missense mutation c.773C>T (p.S258F) in exon 2 of the gap junction protein alpha 8 gene (GJA8) was identified in the proband with nuclear cataract. PMID: 25301372
    17. structural bases of the varied functional consequences of Cx50 missense mutations, were determined. PMID: 25003127
    18. Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1. PMID: 24281366
    19. The results provide a molecular basis for the formation of various cataract phenotypes in human patients with Cx50 mutations. PMID: 24005045
    20. a novel G>A mutation of GJA8 in a three-generation Chinese pedigree was associated with perinuclear opacities of the lens involving the nucleus PMID: 23555834
    21. Data indicate that after inhibition of new protein synthesis with cycloheximide, CX50fs disappeared much more rapidly than CX50, suggesting increased degradation of the mutant. PMID: 23720739
    22. A novel connexin 50 gene (GJA8) mutation, resulting in the amino substitution p. D47H in a Chinese family with nuclear and zonular pulverulent congenital cataracts, is reported. PMID: 23592913
    23. A PDZ-binding motif and ZO-1 protein are necessary for Cx50 intercellular channel formation PMID: 21965293
    24. A missense D47N mutation in GJA8 is associated with autosomal dominant congenital cataract in a Chinese family. PMID: 21921990
    25. Mutations in GJA8 and CRYAA were identified in three Chinese families with cataract and microcornea. PMID: 21686328
    26. The G46V and W45S mutations of connexin 50 are in adjacent amino acids. W45S inhibits gap junctional channel function while G46V reduces cell viability by forming open hemichannels. PMID: 21228318
    27. Two novel nonsynonymous variations and four reported variations in CRYAB, CRYGC, CRYGD, and GJA8, were observed. PMID: 21423869
    28. the gap junction protein-alpha 8 polymorphisms may have a role in age-related cataracts PMID: 20582632
    29. The D47N mutation of Cx50 causes the hereditary nuclear cataract in this family in an autosomal dominant mode of inheritance with incomplete penetrance. PMID: 21174522
    30. This report is the first to relate p.R198W mutation in GJA8 with congenital cataract-microcornea syndrome. PMID: 20806042
    31. This study has identified a novel missense mutation located in the carboxyl terminus of GJA8 (S258F) associated with autosomal dominant nuclear cataract. PMID: 20597646
    32. A novel mutation in GJA8 was detected in a Chinese family with autosomal dominant congenital nuclear cataract, providing clear evidence of a relationship between the genotype and the corresponding cataract phenotype. PMID: 20019893
    33. the C-terminus of human Cx50 is involved in pHi sensitivity, but has little influence over single-channel conductance, voltage dependence, or gating kinetics. PMID: 11944087
    34. Study confirmed that GJA8 plays a vital role in the maintenance of human lens transparency and its mutation could be the genetic defect causing autosomal dominant congenital cataract . PMID: 15696487
    35. The pulverulent cataract described in this family is associated with a novel GJA8 mutation and has a different clinical phenotype from previously described GJA8 mutants. PMID: 16397066
    36. This is the first report of mutations in GJA8 (connexin50) to be associated with autosomal dominant cataract and microcornea. PMID: 16604058
    37. Resultsdemonstrated that Cx50 hemichannels gating control can be cooperated by CaM and Ca2+. PMID: 16740131
    38. Matched case-control and family study indicate that Cx50 may play a role in the genetic susceptibility to schizophrenia. PMID: 17412882
    39. Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract. PMID: 17601931
    40. Five novel mutations in CRYAA, CRYGD, and GJA8 genes were detected in congenital cataract in association with microcornea PMID: 17724170
    41. Pulverulent cataracts present in members of a family are associated with a novel mutation, Cx50D47N, that acts as a loss-of-function mutation. The consequent decrease in lens intercellular communication may contribute to cataract formation. PMID: 18006672
    42. A novel disease-causing mutation (D47Y) of GJA8 gene in a Chinese family with ADCC is reported. PMID: 18247306
    43. This is a novel mutation identified in the first transmembrane domain (M1) of GJA8. PMID: 18334946
    44. A novel GJA8 gene mutation was found to be associated with hereditary cataract in a Chinese congenital cataract family. PMID: 18334966
    45. The ins776G mutation most likely causes a recessive triangular cataract with variable expressivity of a weak phenotype in heterozygotes. PMID: 18483562
    46. A p.P88Q mutation in GJA8 associated with Y-sutural cataract in a family of Indian origin, is reported. PMID: 18587493
    47. The biochemical results indirectly suggest a potential novel mechanism by which connexin mutants could lead to cataracts. PMID: 19684000
    48. Direct sequencing of the PCR product produced from lens cDNA showed that the proband was heterozygous for a G>T transition at position 741 of the GJA8 gene, encoding the exchange of methionine for isoleucine at position 247 of CX50. PMID: 19756179

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  • 相关疾病：
    Cataract 1, multiple types (CTRCT1)
  • 亚细胞定位：
    Cell membrane; Multi-pass membrane protein. Cell junction, gap junction.
  • 蛋白家族：
    Connexin family, Alpha-type (group II) subfamily
  • 组织特异性：
    Eye lens.
  • 数据库链接：

    HGNC: 4281

    OMIM: 116200

    KEGG: hsa:2703

    STRING: 9606.ENSP00000240986

    UniGene: Hs.632441