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C5orf51 抗体

C5orf51 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1385413
发货至: 中国
  • 抗原 See all C5orf51 products
    C5orf51 (Chromosome 5 Open Reading Frame 51 (C5orf51))
    适用
    人, 小鼠, 大鼠
    宿主
    • 5
    • 2
    克隆类型
    • 7
    多克隆
    标记
    • 3
    • 2
    • 1
    • 1
    This C5orf51 antibody is un-conjugated
    应用范围
    • 4
    • 2
    • 2
    • 1
    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 C5orf51
    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
    C5orf51 (Chromosome 5 Open Reading Frame 51 (C5orf51))
    别名
    C5orf51 (C5orf51 产品)
    别名
    chromosome 5 open reading frame 51 antibody, C5orf51 antibody
    背景

    Synonyms: Chromosome 5 open reading frame 51, Hypothetical protein LOC285636, UPF0600 protein C5orf51, CE051_HUMAN.

    Background: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The LOC285636 gene product has been provisionally designated LOC285636 pending further characterization.

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