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EVC2 抗体

EVC2 适用: 人, 小鼠 ELISA, IHC, WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7243292
发货至: 中国
  • 抗原 See all EVC2 抗体
    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
    适用
    人, 小鼠
    宿主
    • 14
    • 1
    克隆类型
    • 15
    多克隆
    标记
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This EVC2 antibody is un-conjugated
    应用范围
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human EVC2
    亚型
    IgG
    Top Product
    Discover our top product EVC2 Primary Antibody
  • 应用备注
    WB 1:200-1:1000, IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.5 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
    别名
    EVC2 (EVC2 产品)
    别名
    EVC2 antibody, LBN antibody, 1110017L09Rik antibody, Lbn antibody, limbin antibody, EvC ciliary complex subunit 2 antibody, EVC2 antibody, Evc2 antibody
    背景
    This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants.
    分子量
    148 kDa
    NCBI登录号
    NP_667338
    UniProt
    Q86UK5
    途径
    Hedgehog Signaling
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