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PRRX1 Antibody

  • 中文名稱:
    PRRX1兔多克隆抗體
  • 貨號:
    CSB-PA188829
  • 規格:
    ¥2024
  • 圖片:
    • Western blot analysis of extracts from NIH-3T3/K562 cells, using PRRX1 antibody.
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) PRRX1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    PRRX1
  • 宿主:
    Rabbit
  • 反應種屬:
    Human,Mouse,Rat
  • 免疫原:
    Synthesized peptide derived from Internal of Human PRRX1.
  • 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.
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA,WB
  • 推薦稀釋比:
    Application Recommended Dilution
    WB 1:500-1:3000
  • 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.

產品評價

靶點詳情

  • 功能:
    Acts as a transcriptional regulator of muscle creatine kinase (MCK) and so has a role in the establishment of diverse mesodermal muscle types. The protein binds to an A/T-rich element in the muscle creatine enhancer.
  • 基因功能參考文獻:
    1. Low PRRX1 expression is associated with hepatocellular carcinoma. PMID: 28677793
    2. identified a functional genetic variant that alters PRRX1 expression, ultimately resulting in electrophysiological alterations in atrial myocytes that may promote Atrial fibrillation. PMID: 28974514
    3. The glioma-initiating cells self-renewal function regulated by PRRX1 is mediated by dopamine D2 receptor (DRD2). PRRX1 directly binds to the DRD2 promoter and transactivates its expression in glioma-initiating cells. PMID: 28486630
    4. LGR5-expressing fraction of CD54+ cells represents gastric cancer CSCs, in which LGR5 is closely associated with stemness and EMT core genes PMID: 28033430
    5. Prrx1b may be an important regulator of epithelial-mesenchymal transition in Triple-negative breast cancer cells. PMID: 27027510
    6. miR-655 inhibits the acquisition of the epithelial-mesenchymal transition phenotype in triple-negative breast cancer by down-regulating Prrx1, thereby inhibiting cell migration and invasion during cancer progression. PMID: 26820102
    7. Decreased Expression of PRRX1 was Associated with Hepatocellular Carcinoma. PMID: 25404478
    8. the switch from Prrx1b to Prrx1a governs EMT plasticity in both mouse models of PDAC and human PDAC PMID: 26773005
    9. These findings demonstrate that PRRX1 promotes epithelial-mesenchymal transition in gastric cancer cells PMID: 25428393
    10. Our results indicate that activation of Notch signaling by PRRX1 is associated with the promotion of glioblastoma cell invasion. PMID: 25522823
    11. We conclude that miR-146b-5p has a role in cell proliferation and invasion, and that PRRX1 plays an important role in papillary thyroid carcinoma epithelial-mesenchymal transition and disease progression. PMID: 24946010
    12. Overexpression of PRRX1 in stably overexpressed-miR-124 cell lines could rescue the effects of radiosensitivity enhancement brought by miR-124. PMID: 24705396
    13. In the rare variant joint analysis, damaging variants within the PRRX1 region showed significant association with AF. PMID: 24239840
    14. PRRX1 is an indicator of metastasis and poor prognosis in colorectal cancer cases. PMID: 23807160
    15. The homeobox factor Prrx1 is an EMT inducer conferring migratory and invasive properties. PMID: 23201163
    16. We show that the homeobox factor Prrx1 is an EMT inducer conferring migratory and invasive properties. The loss of Prrx1 is required for cancer cells to metastasize in vivo, which revert to the epithelial phenotype concomitant with the acquisition of stem cell properties. PMID: 23201163
    17. Mutation analysis was performed after sequencing the entire coding regions of OTX2 and PRRX1 genes isolated from the proband and his parents. After thorough analysis, no DNA variations were detected. PMID: 22198066
    18. identification of the two Prx1 target genes, which play a pivotal role in development of liver fibrosis, is a novel finding for liver pathophysiology PMID: 18296734

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  • 相關疾?。?/div>
    Agnathia-otocephaly complex (AGOTC)
  • 亞細胞定位:
    Nucleus.
  • 蛋白家族:
    Paired homeobox family
  • 數據庫鏈接:

    HGNC: 9142

    OMIM: 167420

    KEGG: hsa:5396

    STRING: 9606.ENSP00000239461

    UniGene: Hs.283416



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