SH3PXD2B Antibody Blocking Peptide(bs-21174P)-500ug

SH3PXD2B Antibody Blocking Pep

tide(bs-21174P)-500ug
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  • bs-21174P
  • 2025年10月16日
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      500ug

    产品编号bs-21174P
    英文名称SH3PXD2B Antibody Blocking Peptide
    中文名称脂肪细胞分化因子49封闭多肽
    英文别名Adapter protein HOFI; Factor for adipocyte differentiation 49; FAD49; FLJ20831; FTHS; KIAA1295; SH3 and PX domain-containing protein 2B; SH3PXD2B; SPD2B_HUMAN; TKS4; Tyrosine kinase substrate with four SH3 domains.
    纯化方法HPLC
    研究领域

    Developmental Biology > Organogenesis > Skeletal development > Bone

    Signal Transduction > Adapters > Cytoplasmic

    Signal Transduction > Cytoskeleton / ECM > Extracellular Matrix > ECM Enzymes > ADAM Protein Family

    亚细胞定位Cytoplasm. Cell projection > podosome. Cytoplasmic in normal cells and localizes to podosomes in SRC-transformed cells.
    组织特异性Expressed in fibroblasts.
    翻译后修饰Phosphorylated in SRC-transformed cells.
    相似性Belongs to the SH3PXD2 family.
    Contains 1 PX (phox homology) domain.
    Contains 4 SH3 domains.
    功能Adapter protein involved in invadopodia and podosome formation and extracellular matrix degradation. Binds matrix metalloproteinases (ADAMs), NADPH oxidases (NOXs) and phosphoinositides. Acts as an organizer protein that allows NOX1- or NOX3-dependent reactive oxygen species (ROS) generation and ROS localization. Plays a role in mitotic clonal expansion during the immediate early stage of adipocyte differentiation (By similarity).
    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 gene encodes an adapter protein that is characterized by a PX domain and four Src homology 3 domains. The encoded protein is required for podosome formation and is involved in cell adhesion and migration of numerous cell types. Mutations in this gene are the cause of Frank-ter Haar syndrome (FTHS), and also Borrone Dermato-Cardio-Skeletal (BDCS) syndrome. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]

     

     

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