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C4orf22 抗体 (Biotin)

This anti-C4orf22 antibody is a 兔 多克隆 antibody detecting C4orf22 in WB 和 IHC (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN1405819
发货至: 中国

Quick Overview for C4orf22 抗体 (Biotin) (ABIN1405819)

抗原

C4orf22 (Chromosome 4 Open Reading Frame 22 (C4orf22))

适用

  • 19
  • 18
  • 16
  • 2
  • 2
  • 1
人, 小鼠, 大鼠

宿主

  • 18
  • 1

克隆类型

  • 18
  • 1
多克隆

标记

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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C4orf22 antibody is conjugated to Biotin

应用范围

  • 19
  • 13
  • 3
  • 1
  • 1
Western Blotting (WB), 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 C4orf22

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400

    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

    C4orf22 (Chromosome 4 Open Reading Frame 22 (C4orf22))

    别名

    C4orf22

    背景

    Synonyms: Chromosome 4 open reading frame 22, Hypothetical protein LOC255119, MGC35043, Uncharacterized protein C4orf22, CD022_HUMAN.

    Background: C4orf22 is a 233 amino acid protein that exists as three alternatively spliced isoforms and are encoded by a gene encoding maping to human chromosome 4, which represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that maps to chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

    基因ID

    255119
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