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RASSF8 抗体

RASSF8 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7003799
发货至: 中国
  • 抗原 See all RASSF8 抗体
    RASSF8 (Ras Association (RalGDS/AF-6) Domain Family (N-terminal) Member 8 (RASSF8))
    适用
    • 53
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    人, 小鼠
    宿主
    • 47
    • 5
    • 1
    克隆类型
    • 50
    • 3
    多克隆
    标记
    • 23
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    This RASSF8 antibody is un-conjugated
    应用范围
    • 47
    • 22
    • 13
    • 13
    • 13
    • 5
    • 5
    • 3
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of human RASSF8
    亚型
    IgG
    Top Product
    Discover our top product RASSF8 Primary Antibody
  • 应用备注
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.5 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    RASSF8 (Ras Association (RalGDS/AF-6) Domain Family (N-terminal) Member 8 (RASSF8))
    别名
    RASSF8 (RASSF8 产品)
    别名
    c12orf2 antibody, rassf8 antibody, wu:fb96e06 antibody, zgc:64017 antibody, C12orf2 antibody, HOJ1 antibody, 5133400D11Rik antibody, AA815821 antibody, AW123240 antibody, Hoj1 antibody, mHoj-1 antibody, RGD1308820 antibody, Ras association domain family member 8 antibody, Ras association (RalGDS/AF-6) domain family (N-terminal) member 8b antibody, Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 antibody, RASSF8 antibody, rassf8b antibody, Rassf8 antibody
    背景
    This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12,22)(p11.2,q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    UniProt
    Q8NHQ8
    途径
    Chromatin Binding
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