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C7ORF26 抗体 (AA 1-100) (Biotin)

C7ORF26 适用: 人 WB, ELISA, IHC (fro), IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1700542
发货至: 中国
  • 抗原 See all C7ORF26 products
    C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))
    抗原表位
    • 14
    • 1
    • 1
    AA 1-100
    适用
    • 16
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 16
    克隆类型
    • 16
    多克隆
    标记
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C7ORF26 antibody is conjugated to Biotin
    应用范围
    • 16
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    预测反应
    Human,Mouse,Rat,Dog,Cow,Chicken,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C7orf26
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    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 for 12 months.
    有效期
    12 months
  • 抗原
    C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))
    别名
    C7orf26 (C7ORF26 产品)
    别名
    C14H7orf26 antibody, zgc:77458 antibody, c7orf26 antibody, chromosome 7 open reading frame 26 antibody, chromosome 14 C7orf26 homolog antibody, zgc:56409 antibody, chromosome 7 open reading frame 26 L homeolog antibody, chromosome 25 open reading frame, human C7orf26 antibody, C7orf26 antibody, C14H7orf26 antibody, zgc:56409 antibody, c7orf26.L antibody, C25H7orf26 antibody
    背景

    Synonyms: Chromosome 7 open reading frame 26, MGC2718, Uncharacterized protein C7orf26,CG026_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 C7orf26 gene product has been provisionally designated C7orf26 pending further characterization.

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