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C10orf2 抗体

C10ORF2 适用: 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7256978
发货至: 中国
  • 抗原 See all C10orf2 (C10ORF2) 抗体
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    适用
    • 43
    • 13
    • 12
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    小鼠
    宿主
    • 41
    • 2
    克隆类型
    • 41
    • 2
    多克隆
    标记
    • 16
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This C10orf2 antibody is un-conjugated
    应用范围
    • 26
    • 19
    • 17
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    A synthetic peptide of human C10orf2 (NP_068602.2).
    亚型
    IgG
    Top Product
    Discover our top product C10ORF2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    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
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    别名
    C10orf2 (C10ORF2 产品)
    别名
    ATXN8 antibody, IOSCA antibody, MTDPS7 antibody, PEO antibody, PEO1 antibody, PEOA3 antibody, SANDO antibody, SCA8 antibody, TWINL antibody, C6H10orf2 antibody, D19Ertd626e antibody, Twinl antibody, twinkle mtDNA helicase L homeolog antibody, twinkle mtDNA helicase antibody, twnk.L antibody, TWNK antibody, Twnk antibody
    背景
    This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
    分子量

    Observed_MW: 77 kDa

    Calculated_MW: 60 kDa/66 kDa/77 kDa

    基因ID
    56652
    UniProt
    Q96RR1
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