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NDE1 抗体

NDE1 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, IP 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5700144
发货至: 中国
  • 抗原 See all NDE1 抗体
    NDE1
    适用
    • 19
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 16
    • 3
    克隆类型
    • 16
    • 3
    多克隆
    标记
    • 14
    • 1
    • 1
    • 1
    • 1
    • 1
    This NDE1 antibody is un-conjugated
    应用范围
    • 17
    • 12
    • 4
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
    免疫原
    nudE nuclear distribution gene E homolog 1 (A. nidulans)
    亚型
    IgG
    Top Product
    Discover our top product NDE1 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    说明

    A2780 cells were subjected to SDS PAGE followed by western blot with FNab05600(NDE1 antibody) at dilution of 1:1500

    限制
    仅限研究用
  • 缓冲液
    PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3
    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
    有效期
    12 months
  • 抗原
    NDE1
    别名
    NDE1 (NDE1 产品)
    别名
    2810027M15Rik antibody, AU042936 antibody, AW822251 antibody, Nude antibody, mNudE antibody, HOM-TES-87 antibody, LIS4 antibody, NDE antibody, NUDE antibody, NUDE1 antibody, fb82g01 antibody, im:7141877 antibody, wu:fb82g01 antibody, zgc:114109 antibody, nudE neurodevelopment protein 1 antibody, Nde1 antibody, NDE1 antibody, nde1 antibody
    背景
    Synonyms:NUDE Background:This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe mental retardation. Alternative splicing results in multiple transcript variants.
    分子量
    40 kDa
    基因ID
    54820
    UniProt
    Q9NXR1
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