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C2orf24 抗体

C2orf24 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1387180
发货至: 中国
  • 抗原 See all C2orf24 products
    C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))
    适用
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 3
    克隆类型
    • 3
    多克隆
    标记
    • 3
    This C2orf24 antibody is un-conjugated
    应用范围
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C2orf24
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
    4 °C,-20 °C
    储存方法
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    有效期
    12 months
  • 抗原
    C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))
    别名
    C2orf24 (C2orf24 产品)
    别名
    c2orf24 antibody, wu:fa05h07 antibody, zgc:55857 antibody, MGC75999 antibody, C12H2orf24 antibody, MGC115028 antibody, DKFZp459J1014 antibody, C2orf24 antibody, CGI-57 antibody, C2H2orf24 antibody, C7H2orf24 antibody, 1810031K17Rik antibody, AU043960 antibody, RGD735175 antibody, cyclin Pas1/PHO80 domain containing 1 antibody, cyclin Pas1/PHO80 domain containing 1 L homeolog antibody, cnppd1 antibody, CNPPD1 antibody, cnppd1.L antibody, Cnppd1 antibody
    背景

    Synonyms: CDABP0125, CGI 57, chromosome 2 open reading frame 24, CNPD1_HUMAN, CNPPD1, Cyclin Pas1/PHO80 domain-containing protein 1, Protein CNPPD1.

    Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf24 gene product has been provisionally designated C2orf24 pending further characterization.

    基因ID
    27013
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