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C8orf47 抗体 (Cy7)

C8ORF47 适用: 人 WB 宿主: 兔 Polyclonal Cy7
产品编号 ABIN1707333
发货至: 中国
  • 抗原 See all C8orf47 (C8ORF47) products
    C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))
    适用
    宿主
    • 14
    克隆类型
    • 14
    多克隆
    标记
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    This C8orf47 antibody is conjugated to Cy7
    应用范围
    Western Blotting (WB)
    交叉反应
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C8orf47
    亚型
    IgG
  • 应用备注
    IF(IHC-P) 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
    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))
    别名
    C8orf47 (C8ORF47 产品)
    别名
    glutamate rich 5 antibody, ERICH5 antibody
    背景

    Synonyms: C8orf47, CH047_HUMAN, Chromosome 8 open reading frame 47, Uncharacterized protein C8orf47.

    Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf47 gene product has been provisionally designated C8orf47 pending further characterization.

    基因ID
    203111
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