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C8orf12 抗体 (AA 1-80) (Biotin)

C8ORF12 适用: 人 IHC (p), ELISA, IHC (fro) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1699936
发货至: 中国
  • 抗原 See all C8orf12 (C8ORF12) products
    C8orf12 (C8ORF12) (Chromosome 8 Open Reading Frame 12 (C8ORF12))
    抗原表位
    AA 1-80
    适用
    宿主
    • 14
    克隆类型
    • 14
    多克隆
    标记
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C8orf12 antibody is conjugated to Biotin
    应用范围
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro))
    交叉反应
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C8orf12
    亚型
    IgG
  • 应用备注
    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
    C8orf12 (C8ORF12) (Chromosome 8 Open Reading Frame 12 (C8ORF12))
    别名
    C8orf12 (C8ORF12 产品)
    别名
    FAM167A antisense RNA 1 antibody, FAM167A-AS1 antibody
    背景

    Synonyms: Chromosome 8 open reading frame 12, Uncharacterized protein C8orf12, CH012_HUMAN.

    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 C8orf12 gene product has been provisionally designated C8orf12 pending further characterization.

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