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PEX2 Antibody

  • 中文名稱:
    PEX2兔多克隆抗體
  • 貨號:
    CSB-PA985453
  • 規(guī)格:
    ¥2024
  • 圖片:
    • Western blot analysis of extracts from A549 cells, using PXMP3 antibody.
    • Immunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue using PXMP3 antibody.
  • 其他:

產(chǎn)品詳情

  • 產(chǎn)品名稱:
    Rabbit anti-Homo sapiens (Human) PEX2 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    PEX2
  • 別名:
    PEX2; PAF1; PMP3; PMP35; PXMP3; RNF72; Peroxisome biogenesis factor 2; 35 kDa peroxisomal membrane protein; Peroxin-2; Peroxisomal membrane protein 3; Peroxisome assembly factor 1; PAF-1; RING finger protein 72
  • 宿主:
    Rabbit
  • 反應(yīng)種屬:
    Human
  • 免疫原:
    Synthesized peptide derived from N-terminal of Human PXMP3.
  • 免疫原種屬:
    Homo sapiens (Human)
  • 克隆類型:
    Polyclonal
  • 純化方式:
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 產(chǎn)品提供形式:
    Liquid
  • 應(yīng)用范圍:
    ELISA,WB,IHC
  • 推薦稀釋比:
    Application Recommended Dilution
    WB 1:500-1:3000
    IHC 1:50-1:100
  • Protocols:
  • 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(chǎn)品評價(jià)

靶點(diǎn)詳情

  • 功能:
    Somewhat implicated in the biogenesis of peroxisomes.
  • 基因功能參考文獻(xiàn):
    1. PEX2 is required for peroxisome autophagy during starvation. PMID: 27597759
    2. the carrier frequencies for two PEX2 mutations causative of the severe Zellweger syndrome spectrum phenotype in Ashkenazi Jews PMID: 23590336
    3. Ischemic wound healing is retarded in mice subjected to recombinant PEX2 injections or viral transduction with PEX2-lentivurus. PMID: 21903356
    4. Genetic screening of PEX2 and other PEX genes involved in peroxisomal biogenesis is warranted in children and adults with ARCA PMID: 21392394
    5. The cause of the syndrome in this patient was a point mutation that resulted in the premature termination of peroxisome assembly factor-1. PMID: 1546315

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  • 相關(guān)疾病:
    Peroxisome biogenesis disorder complementation group 5 (PBD-CG5); Peroxisome biogenesis disorder 5A (PBD5A); Peroxisome biogenesis disorder 5B (PBD5B)
  • 亞細(xì)胞定位:
    Peroxisome membrane; Multi-pass membrane protein.
  • 蛋白家族:
    Pex2/pex10/pex12 family
  • 數(shù)據(jù)庫鏈接:

    HGNC: 9717

    OMIM: 170993

    KEGG: hsa:5828

    STRING: 9606.ENSP00000349543

    UniGene: Hs.437966



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