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CCM2 抗体 (N-Term)

CCM2 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN616006
发货至: 中国
  • 抗原 See all CCM2 抗体
    CCM2 (Cerebral Cavernous Malformation 2 (CCM2))
    抗原表位
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 1-444, N-Term
    适用
    • 23
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 18
    • 4
    • 1
    克隆类型
    • 22
    • 1
    多克隆
    标记
    • 16
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CCM2 antibody is un-conjugated
    应用范围
    • 13
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    特异性
    This antibody detects recombinant Human CCM-2 in Western Blot and native CCM-2 in Immunohistochemistry.
    交叉反应 (详细)
    Species reactivity (tested):Human.
    纯化方法
    Protein A Chromatography
    免疫原
    Highly pure (> 95%) recombinant Human CCM-2 (Cerebral cavernous malformations 2 protein, aa: Met1-Ala444) from E.coli.
    Top Product
    Discover our top product CCM2 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 溶解方式
    Restore in sterile water to a concentration of 0.1-1.0 mg/mL.
    缓冲液
    5 mM PBS pH 7.2 without preservatives
    储存液
    Without preservative
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Prior to reconstitution store at 2-8 °C for one month or dessicated at -20 °C for longer. Following reconstitution store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原
    CCM2 (Cerebral Cavernous Malformation 2 (CCM2))
    别名
    Malcavernin (CCM2 产品)
    别名
    C7orf22 antibody, OSM antibody, malcavernin antibody, CCM2 antibody, BC029157 antibody, TUF2 antibody, vtn antibody, zgc:110233 antibody, CCM2 scaffolding protein antibody, cerebral cavernous malformation 2 antibody, malcavernin antibody, CCM2 antibody, Ccm2 antibody, LOC100304744 antibody, ccm2 antibody
    背景
    Cerebral cavernous malformations (CCMs) are sporadically acquired or inherited vascular lesions of the central nervous system consisting of clusters of dilated thin-walled blood vessels that predispose individuals to seizures and stroke. Familial CCM is caused by mutations in KRIT1 (CCM1) or in malcavernin (CCM2). The roles of the CCM proteins in the pathogenesis of the disorder remain largely unknown. It was shown that the CCM1 gene product, KRIT1, interacts with the CCM2 gene product, malcavernin. Analogous to the established interactions of CCM1 and beta1 integrin with ICAP1, the CCM1/CCM2 association is dependent upon the phosphotyrosine binding (PTB) domain of CCM2. A familial CCM2 missense mutation abrogates the CCM1/CCM2 interaction, suggesting that loss of this interaction may be critical in CCM pathogenesis. CCM2 and ICAP1 bound to CCM1 via their respective PTB domains differentially influence the subcellular localization of CCM1. The data indicate that the genetic heterogeneity observed in familial CCM may reflect mutation of different molecular members of a coordinated signaling complex.Synonyms: C7orf22, CCM2, Cerebral cavernous malformations 2 protein, PP10187
    基因ID
    83605
    NCBI登录号
    NP_001025006
    UniProt
    Q9BSQ5
    途径
    Cell-Cell Junction Organization
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