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C4ORF32 抗体 (AbBy Fluor® 647)

This anti-C4ORF32 antibody is a 兔 多克隆 antibody detecting C4ORF32 in WB 和 IF (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN1405842
发货至: 中国

Quick Overview for C4ORF32 抗体 (AbBy Fluor® 647) (ABIN1405842)

抗原

C4ORF32 (Chromosome 4 Open Reading Frame 32 (C4ORF32))

适用

人, 小鼠, 大鼠

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 C4ORF32 antibody is conjugated to AbBy Fluor® 647

应用范围

  • 14
  • 12
  • 3
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (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 C4orf32

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200

    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    C4ORF32 (Chromosome 4 Open Reading Frame 32 (C4ORF32))

    别名

    C4orf32

    背景

    Synonyms: C4orf32, CD032_HUMAN, Chromosome 4 open reading frame 32, FLJ39370, Uncharacterized protein C4orf32.

    Background: C4orf32 is a 132 amino acid single pass membrane protein that is encoded by a gene that maps to human chromosome 4. Human chromosome 4 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 located on chromosome 4. FGFR-3 is also encoded by a gene that maps to human 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.

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