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CC2D2A 抗体 (N-Term)

CC2D2A 适用: 人, 小鼠, 豚鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2790202
发货至: 中国
  • 抗原 See all CC2D2A 抗体
    CC2D2A (Coiled-Coil and C2 Domain Containing 2A (CC2D2A))
    抗原表位
    N-Term
    适用
    人, 小鼠, 豚鼠
    宿主
    • 2
    克隆类型
    • 2
    多克隆
    标记
    • 2
    This CC2D2A antibody is un-conjugated
    应用范围
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    序列
    EDADMGRQNK NSKVRRQPRK KQKPTPFSRA CWQILPHLSA GVPLLGWEHP
    预测反应
    Guinea Pig: 77%, Human: 100%, Mouse: 92%
    产品特性
    This is a rabbit polyclonal antibody against CC2D2A. It was validated on Western Blot.
    纯化方法
    Affinity Purified
    免疫原
    The immunogen is a synthetic peptide directed towards the N-terminal region of Human CC2D2A
    Top Product
    Discover our top product CC2D2A Primary Antibody
  • 应用备注
    Optimal working dilutions should be determined experimentally by the investigator.
    说明

    Antigen size: 122 AA

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    Lot specific
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原
    CC2D2A (Coiled-Coil and C2 Domain Containing 2A (CC2D2A))
    别名
    CC2D2A (CC2D2A 产品)
    别名
    JBTS9 antibody, MKS6 antibody, 5730509K17Rik antibody, b2b1035Clo antibody, fc03c12 antibody, wu:fc03c12 antibody, RGD1561042 antibody, coiled-coil and C2 domain containing 2A antibody, coiled-coil and C2 domain containing 2A L homeolog antibody, CC2D2A antibody, Cc2d2a antibody, cc2d2a.L antibody, cc2d2a antibody
    背景
    This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants.
    Alias Symbols: JBTS9, KIAA1345, MKS6
    Protein Interaction Partner: UBC,
    Protein Size: 122
    分子量
    14 kDa
    基因ID
    57545
    NCBI登录号
    NM_020785, NP_065836
    UniProt
    E7EP21
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