PAX3 Antibody Blocking Peptide(bs-1097P)-500ug

PAX3 Antibody Blocking Peptide

(bs-1097P)-500ug
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  • bs-1097P
  • 2025年10月16日
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      500ug

    产品编号bs-1097P
    英文名称PAX3 Antibody Blocking Peptide
    中文名称配对盒基因3封闭多肽
    英文别名CDHS; HUP 2; HUP2; MGC120381; MGC120382; MGC120383; MGC120384; MGC134778; paired box homeotic gene 3; Paired box protein Pax 3; Paired box protein Pax3; paired domain gene 3; paired domain gene HuP2; PAX 3; PAX3/FKHR fusion gene; Waardenburg syndrome 1; WS 1; WS1.
    纯化方法HPLC
    研究领域

    Developmental Biology > Lineage specification > Ectoderm

    Developmental Biology > Organogenesis > Nervous system development

    Epigenetics and Nuclear Signaling > Transcription > Domain Families > Developmental Families > PAX

    Stem Cells > Lineage Markers > Ectoderm

    Stem Cells > Mesenchymal Stem Cells > Myogenesis

    Stem Cells > Neural Stem Cells > Intracellular

    Stem Cells > Neural Stem Cells > Neural Crest Stem Cells

    亚基Can bind to DNA as a homodimer or a heterodimer with PAX7. Interacts with PAXBP1; the interaction links PAX3 to a WDR5-containing histone methyltransferase complex. Interacts with DAXX.
    亚细胞定位Nucleus.
    相似性Belongs to the paired homeobox family.
    Contains 1 homeobox DNA-binding domain.
    Contains 1 paired domain.
    功能Transcription factor that may regulate cell proliferation, migration and apoptosis. Involved in neural development and myogenesis.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料This protein is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These proteins play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t(2;13)(q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma. Alternative splicing results in transcripts encoding isoforms with different C-termini.

     

     

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