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C7orf10 抗体 (AA 351-445) (Cy5)

C7orf10 适用: 人 WB, IF (cc), IF (p) 宿主: 兔 Polyclonal Cy5
产品编号 ABIN1704629
发货至: 中国
  • 抗原 See all C7orf10 抗体
    C7orf10 (Chromosome 7 Open Reading Frame 10 (C7orf10))
    抗原表位
    • 14
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 351-445
    适用
    • 21
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 17
    • 4
    克隆类型
    • 19
    • 2
    多克隆
    标记
    • 8
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C7orf10 antibody is conjugated to Cy5
    应用范围
    • 19
    • 12
    • 12
    • 6
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    预测反应
    Human,Mouse,Rat,Dog,Cow,Sheep,Horse,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C7orf10
    亚型
    IgG
    Top Product
    Discover our top product C7orf10 Primary Antibody
  • 应用备注
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    C7orf10 (Chromosome 7 Open Reading Frame 10 (C7orf10))
    别名
    C7orf10 (C7orf10 产品)
    别名
    DERP13 antibody, ORF19 antibody, c7orf10 antibody, sugct antibody, succinyl-CoA:glutarate-CoA transferase antibody, succinyl-CoA:glutarate-CoA transferase L homeolog antibody, SUGCT antibody, sugct.L antibody
    背景

    Synonyms: Chromosome 7 open reading frame 10, Dermal papilla derived protein 13, DERP13, FLJ11808, Hypothetical protein LOC79783, ORF19, Russel-Silver syndrome candidate, Uncharacterized protein C7orf10,CG010_HUMAN.

    Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterization.

    基因ID
    79783
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