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C7ORF25 抗体 (AA 1-100) (Cy7)

C7ORF25 适用: 小鼠 WB, IF (cc), IF (p) 宿主: 兔 Polyclonal Cy7
产品编号 ABIN1708590
发货至: 中国
  • 抗原 See all C7ORF25 products
    C7ORF25 (Chromosome 7 Open Reading Frame 25 (C7ORF25))
    抗原表位
    • 14
    • 14
    • 7
    AA 1-100
    适用
    • 14
    • 14
    小鼠
    宿主
    • 28
    克隆类型
    • 28
    多克隆
    标记
    • 5
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C7ORF25 antibody is conjugated to Cy7
    应用范围
    • 28
    • 15
    • 13
    • 12
    • 12
    • 5
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    小鼠
    预测反应
    Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C7orf25
    亚型
    IgG
  • 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
    C7ORF25 (Chromosome 7 Open Reading Frame 25 (C7ORF25))
    别名
    C7orf25 (C7ORF25 产品)
    别名
    C7orf25 antibody, c7orf25 antibody, chromosome 7 open reading frame 25 antibody, chromosome 4 open reading frame, human C7orf25 antibody, expressed sequence AW209491 antibody, similar to expressed sequence AW209491 antibody, chromosome 7 open reading frame 25 L homeolog antibody, C7orf25 antibody, C4H7orf25 antibody, AW209491 antibody, RGD1308147 antibody, c7orf25.L antibody
    背景

    Synonyms: C7orf25, CG025_HUMAN, Chromosome 7 open reading frame 25, RGD1308147, UPF0415 protein C7orf25.

    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 C7orf25 gene product has been provisionally designated C7orf25 pending further characterization.

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