HEG1 Antibody Blocking Peptide(bs-15449P)-500ug

HEG1 Antibody Blocking Peptide

(bs-15449P)-500ug
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  • bs-15449P
  • 2025年10月16日
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      500ug

    产品编号bs-15449P
    英文名称HEG1 Antibody Blocking Peptide
    中文名称HEG同源蛋白1封闭多肽
    英文别名HEG; HEG1; HEG1_HUMAN; KIAA1237; MST112; MSTP112; HEG homolog 1; Protein HEG homolog 1.
    纯化方法HPLC
    研究领域

    Cardiovascular > Angiogenesis > Growth Factors

    Cardiovascular > Heart > Cardiogenesis > Transcription factors/regulators

    Developmental Biology > Organogenesis > Angiogenesis and vasculogenesis

    Signal Transduction > Cytoskeleton / ECM > Cell Adhesion > Tight Junctions

    Signal Transduction > Signaling Pathway > Calcium Signaling > Calcium Binding Proteins

    亚基Interacts with CCM2 and KRIT1; KRIT1 markedly facilitates interaction with CCM2.
    亚细胞定位Isoform 1: Cell membrane; Single-pass type I membrane protein (Potential). Cell junction.
    Isoform 2: Secreted (Potential).
    相似性Contains 2 EGF-like domains.
    功能Receptor component of the CCM signaling pathway which is a crucial regulator of heart and vessel formation and integrity May act through the stabilization of endothelial cell junctions.
    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HEG1 (HEG homolog 1) is also known as HEG and is a 1,381 amino acid protein that exists as two alternatively spliced isoforms, one of which is a single-pass membrane protein and the other of which is secreted. HEG1, which is expressed in endothelial cells and smooth muscle cells of heart tissue, contains two EGF-like domains that play a role in calcium-binding events which may regulate concentric heart growth. The gene encoding HEG1 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

     

     

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