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TFB1M Antibody, FITC conjugated

  • 中文名稱:
    TFB1M兔多克隆抗體, FITC偶聯
  • 貨號:
    CSB-PA023420LC01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) TFB1M Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    TFB1M
  • 別名:
    N'-adenosyl(rRNA) dimethyltransferase 1 antibody; CGI75 antibody; Dimethyladenosine transferase 1; mitochondrial antibody; h-mtTFB antibody; h-mtTFB1 antibody; hmtTFB antibody; hmtTFB1 antibody; hTFB1M antibody; Mitochondrial 12S rRNA dimethylase 1 antibody; Mitochondrial dimethyladenosine transferase 1 antibody; Mitochondrial transcription factor B1 antibody; mtTFB1 antibody; S-adenosylmethionine-6-N' antibody; Tfb1m antibody; TFB1M_HUMAN antibody; Transcription factor B1 mitochondrial antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Dimethyladenosine transferase 1, mitochondrial protein (59-194AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    FITC
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 產品提供形式:
    Liquid
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    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.

產品評價

靶點詳情

  • 功能:
    S-adenosyl-L-methionine-dependent methyltransferase which specifically dimethylates mitochondrial 12S rRNA at the conserved stem loop. Also required for basal transcription of mitochondrial DNA, probably via its interaction with POLRMT and TFAM. Stimulates transcription independently of the methyltransferase activity.
  • 基因功能參考文獻:
    1. Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes. PMID: 24916378
    2. Deficiency in TFB1M and impaired mitochondrial function contribute to the pathogenesis of type 2 diabetes. PMID: 21195351
    3. The mRNA levels of TFB1M and TFB2M are influenced by endurance training PMID: 19681768
    4. This transcription factor activates transcription of human mitochondrial DNA. PMID: 12068295
    5. Human mitochondrial transcription factor B1 methylates ribosomal RNA at a conserved stem-loop PMID: 12496758
    6. TFB1 interacts with the C-terminal activation region of h-mtTFA and stimulates transcription independently of its RNA methyltransferase activity PMID: 12897151
    7. TFB1M is a nuclear-encoded modifier gene for phenotypic expression of the deafness-associated homoplasmic A1555G mutation in the mitochondrial 12S rRNA gene. PMID: 15110318
    8. Distinct, but possibly coordinated functions of mtTFB1 and mtTFB2 in mitochondrial gene expression and biogenesis. PMID: 17557812
    9. This study suggested that DNA variants in TFB1M did not contribute to the risk for parkinson disease. PMID: 18980857
    10. determined the variation in the TFAM, TFB1M, and TFB2M genes in cardiac hypertrophy PMID: 19096125
    11. rRNA methyltransferase activity is necessary for induction of mitochondrial biogenesis by TFB1M, but not TFB2M. PMID: 19417006

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  • 相關疾病:
    Variations in TFB1M may influence the clinical expression of aminoglycoside-induced deafness caused by the A1555G mutation in the mitochondrial 12S rRNA.
  • 亞細胞定位:
    Mitochondrion.
  • 蛋白家族:
    Class I-like SAM-binding methyltransferase superfamily, rRNA adenine N(6)-methyltransferase family, KsgA subfamily
  • 組織特異性:
    Ubiquitously expressed.
  • 數據庫鏈接:

    HGNC: 17037

    OMIM: 607033

    KEGG: hsa:51106

    STRING: 9606.ENSP00000356134

    UniGene: Hs.279908



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