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MRPL3 Antibody

  • 货号：
    CSB-PA003294
  • 规格：
    ￥880
  • 图片：
    • Western Blot analysis of Jurkat cells using MRP-L3 Polyclonal Antibody
    • Western Blot analysis of Jurkat cells using MRP-L3 Polyclonal Antibody
  • 其他：

产品详情

  • Uniprot No.：
    P09001
  • 基因名：
    MRPL3
  • 别名：
    39S ribosomal protein L3 antibody; 39S ribosomal protein L3 mitochondrial antibody; COXPD9 antibody; L3mt antibody; Mitochondrial 39S ribosomal protein L3 antibody; Mitochondrial 60S ribosomal protein L3 antibody; mitochondrial antibody; mitochondrial ribosomal protein antibody; Mitochondrial ribosomal protein L3 antibody; MRL3 antibody; MRP-L3 antibody; MRPL3 antibody; RM03_HUMAN antibody; RPML3 antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human
  • 免疫原：
    Synthesized peptide derived from the Internal region of Human MRP-L3.
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    Non-conjugated
  • 抗体亚型：
    IgG
  • 纯化方式：
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 产品提供形式：
    Liquid
  • 应用范围：
    WB, ELISA
  • 推荐稀释比：
    Application Recommended Dilution
    WB 1:500-1:2000
    ELISA 1:5000
  • Protocols：
  • 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.

产品评价

靶点详情

  • 基因功能参考文献：
    1. Found MRPL3 S75N variant is probably a rare cause of Tourette syndrome/chronic tic phenotype in Chinese Han patients. PMID: 22507240
    2. the first mutation in large mitochondrial ribosomal protein MRPL3 in a family of four sibs with hypertrophic cardiomyopathy, psychomotor retardation, and multiple respiratory chain deficiency.(MRPL3) PMID: 21786366
  • 相关疾病：
    Combined oxidative phosphorylation deficiency 9 (COXPD9)
  • 亚细胞定位：
    Mitochondrion.
  • 蛋白家族：
    Universal ribosomal protein uL3 family
  • 数据库链接：

    HGNC: 10379

    OMIM: 607118

    KEGG: hsa:11222

    STRING: 9606.ENSP00000264995

    UniGene: Hs.205163