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Chromosome 5 Open Reading Frame 39 (C5orf39) (AA 50-100) 抗体 (Cy5)

This Cy5-conjugated 兔 多克隆 anti-not_set antibody specifically detects not_set in IF (cc) 和 IF (p). The antibody is reactive with 人 samples.
产品编号 ABIN1415045
发货至: 中国
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Quick Overview for Chromosome 5 Open Reading Frame 39 (C5orf39) (AA 50-100) 抗体 (Cy5) (ABIN1415045)

抗原

See all Chromosome 5 Open Reading Frame 39 (C5orf39) 抗体
Chromosome 5 Open Reading Frame 39 (C5orf39)

适用

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宿主

  • 23
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克隆类型

  • 25
多克隆

标记

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Cy5

应用范围

  • 12
  • 12
  • 5
  • 3
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Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 3
    • 2
    AA 50-100

    预测反应

    Human

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human Annexin-2 receptor

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 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

    Chromosome 5 Open Reading Frame 39 (C5orf39)

    别名

    AX2R

    背景

    Synonyms: LOC389289, ANXA2R, Annexin 2 receptor, Annexin II receptor, AX2R, AXIIR, C5orf39, Chromosome 5 open reading frame 39, AX2R_HUMAN.

    Background: ANXA2R (annexin-2 receptor), also known as AX2R or C5orf39, is a 193 amino acid protein that is widely expressed and may act as an annexin II receptor on marrow stromal cells to induce osteoclast formation. In addition, ANXA2R is highly expressed in lymphocytes and is also found in resting CD4+ and CD8+ T cells. The gene encoding ANXA2R maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6 % of the human genome. Chromosome 5 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, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

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