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C7ORF57 抗体 (AA 161-260) (FITC)

C7ORF57 适用: 大鼠 IF (cc), IF (p) 宿主: 兔 Polyclonal FITC
产品编号 ABIN1710049
发货至: 中国
  • 抗原 See all C7ORF57 products
    C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))
    抗原表位
    • 14
    • 1
    • 1
    AA 161-260
    适用
    • 16
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    大鼠
    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 C7ORF57 antibody is conjugated to FITC
    应用范围
    • 12
    • 12
    • 3
    • 3
    • 3
    • 2
    • 1
    Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    大鼠
    预测反应
    Human,Mouse,Cow,Sheep,Horse
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C7orf57
    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
    C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))
    别名
    C7orf57 (C7ORF57 产品)
    别名
    C7orf57 antibody, chromosome 4 open reading frame, human C7orf57 antibody, chromosome 7 open reading frame 57 antibody, C4H7orf57 antibody, C7orf57 antibody
    背景

    Synonyms: C7orf57, CG057_HUMAN, Chromosome 7 open reading frame 57, Uncharacterized protein C7orf57.

    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 C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.

    基因ID
    136288
    UniProt
    Q8NEG2
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