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  4. HOXA2 Antibody, FITC conjugated

HOXA2 Antibody, FITC conjugated

说明书
  • 中文名称：
    HOXA2兔多克隆抗体, FITC偶联
  • 货号：
    CSB-PA010652LC01HU
  • 规格：
    ￥880
  • 其他：

产品详情

  • 产品名称：
    Rabbit anti-Homo sapiens (Human) HOXA2 Polyclonal antibody
  • Uniprot No.：
    O43364
  • 基因名：
    HOXA2
  • 别名：
    AI324701 antibody; homeo box A2 antibody; homeobox A2 antibody; Homeobox protein Hox-1K antibody; Homeobox protein Hox-A2 antibody; Hox-1.11 antibody; HOX1.11 antibody; HOX1K antibody; Hoxa-2 antibody; Hoxa11 antibody; HOXA2 antibody; HXA2_HUMAN antibody; MGC151482 antibody; MGC151484 antibody; RATHOX111A antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human
  • 免疫原：
    Recombinant Human Homeobox protein Hox-A2 protein (26-124AA)
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    FITC
  • 克隆类型：
    Polyclonal
  • 抗体亚型：
    IgG
  • 纯化方式：
    >95%, Protein G purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
  • 产品提供形式：
    Liquid
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
  • 用途：
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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HOXA2 antibodies

HOXA2 Proteins

靶点详情

  • 功能：
    Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.
  • 基因功能参考文献：
    1. Performed mutational analysis of TCOF1, GSC, and HOXA2 to determine the mutational features of the 3 genes in Chinese patients with Treacher Collins syndrome. PMID: 27526242
    2. The role of HOXA2 gene in dominant isolated microtia and the dysmorphogenetic effect of this gene on ear development PMID: 27503514
    3. 5 genomic variants in GSC, HOXA2 and PRKRA were identified through mutational analysis in Chinese patients with microtia. PMID: 28109504
    4. The Hoxa2-mediated decay of RCHY1 involves both the 19S and 20S proteasome complexes PMID: 26496426
    5. HOXA2 acts as a suppressor or TBP-antagonist to inhibit MMP-9 expression; while methylation-mediated inactivation of HOXA2 in NPC derepresses MMP-9 production and increases invasion of NPC cells. PMID: 24243817
    6. we have identified a nonsense mutation (Q235*) in HOXA2 that segregates with bilateral nonsyndromic microtia and hearing loss through three generations of a family in an autosomal dominant pattern. PMID: 23775976
    7. Lack of mutations in the coding region of HOXA2 among the sporadic microtia patients. PMID: 20542577
    8. A missense mutation in the HOXA2 in a consanguineous iranian family with bilateral microtia was reported. PMID: 18394579

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  • 相关疾病：
    Microtia, hearing impairment, and cleft palate (MHICP); Microtia with or without hearing impairment (MCRT)
  • 亚细胞定位：
    Nucleus.
  • 蛋白家族：
    Antp homeobox family, Proboscipedia subfamily
  • 数据库链接：

    HGNC: 5103

    OMIM: 604685

    KEGG: hsa:3199

    STRING: 9606.ENSP00000222718

    UniGene: Hs.445239

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