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C8ORF44 抗体 (AA 81-159) (Biotin)

C8ORF44 适用: 人 WB, IHC (fro), IHC (p), ELISA 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1699939
发货至: 中国
  • 抗原 See all C8ORF44 products
    C8ORF44 (Chromosome 8 Open Reading Frame 44 (C8ORF44))
    抗原表位
    • 14
    • 2
    • 1
    • 1
    • 1
    AA 81-159
    适用
    宿主
    • 24
    克隆类型
    • 24
    多克隆
    标记
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C8ORF44 antibody is conjugated to Biotin
    应用范围
    • 18
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
    预测反应
    Human
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C8orf44
    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
    C8ORF44 (Chromosome 8 Open Reading Frame 44 (C8ORF44))
    别名
    C8orf44 (C8ORF44 产品)
    别名
    chromosome 8 open reading frame 44 antibody, C8orf44 antibody
    背景

    Synonyms: C8orf44, CH044_HUMAN, FLJ11267, Putative uncharacterized protein C8orf44.

    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 C8orf44 gene product has been provisionally designated C8orf44 pending further characterization.

    基因ID
    56260
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