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ISCU 抗体

ISCU 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7261091
发货至: 中国
  • 抗原 See all ISCU 抗体
    ISCU (Iron-sulfur cluster assembly enzyme ISCU, mitochondrial (ISCU))
    适用
    • 32
    • 13
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 28
    • 4
    克隆类型
    • 28
    • 3
    多克隆
    标记
    • 18
    • 4
    • 3
    • 3
    • 2
    • 2
    This ISCU antibody is un-conjugated
    应用范围
    • 26
    • 22
    • 5
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    A synthetic Peptide of human ISCU
    亚型
    IgG
    Top Product
    Discover our top product ISCU Primary Antibody
  • 应用备注
    WB 1:500-1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 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.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    ISCU (Iron-sulfur cluster assembly enzyme ISCU, mitochondrial (ISCU))
    别名
    ISCU (ISCU 产品)
    别名
    nifun antibody, zC191D15.3 antibody, si:ch211-191d15.3 antibody, 2310020H20Rik antibody, HML antibody, ISU2 antibody, NIFU antibody, NIFUN antibody, hnifU antibody, RGD1309562 antibody, AA407971 antibody, Nifu antibody, Nifun antibody, iron-sulfur cluster assembly enzyme ISCU, mitochondrial antibody, iron-sulfur cluster assembly enzyme antibody, iron-sulfur cluster assembly enzyme a antibody, LOC409130 antibody, ISCU antibody, iscua antibody, Iscu antibody
    背景
    This gene encodes a component of the iron-sulfur (Fe-S) cluster scaffold. Fe-S clusters are cofactors that play a role in the function of a diverse set of enzymes, including those that regulate metabolism, iron homeostasis, and oxidative stress response. Alternative splicing results in transcript variants encoding different protein isoforms that localize either to the cytosol or to the mitochondrion. Mutations in this gene have been found in patients with hereditary myopathy with lactic acidosis. A disease-associated mutation in an intron may activate a cryptic splice site, resulting in the production of a splice variant encoding a putatively non-functional protein. A pseudogene of this gene is present on chromosome 1.
    分子量

    Observed_MW: 26 kDa

    Calculated_MW: 15 kDa/17 kDa

    基因ID
    23479
    UniProt
    Q9H1K1
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