LZTS2 Antibody Blocking Peptide(bs-18601P)-500ug

LZTS2 Antibody Blocking Peptid

e(bs-18601P)-500ug
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  • bs-18601P
  • 2025年10月16日
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      500ug

    产品编号bs-18601P
    英文名称LZTS2 Antibody Blocking Peptide
    中文名称亮氨酸拉链抑癌蛋白2封闭多肽
    英文别名hLZTS2; KIAA1813; LAPSER1; Leucine zipper putative tumor suppressor 2; LZTS2; LZTS2_HUMAN; OTTHUMP00000020289; Protein LAPSER1; RP11-108L7.8.
    纯化方法HPLC
    亚细胞定位Cytoplasm. Cytoplasm, cytoskeleton, centrosome. Localized to the centrosome throughout the cell cycle. Localized to the midbody in cells undergoing cytokinesis.
    组织特异性Highly expressed in prostate and testis, and at slightly lower levels in spleen, thymus, uterus, small intestine and colon.
    相似性Belongs to the LZTS2 family.
    功能Negative regulator of katanin-mediated microtubule severing and release from the centrosome. Required for central spindle formation and the completion of cytokinesis. May negatively regulate axonal outgrowth by preventing the formation of microtubule bundles that are necessary for transport within the elongating axon. Negative regulator of the Wnt signaling pathway. Represses beta-catenin-mediated transcriptional activation by promoting the nuclear exclusion of beta-catenin.
    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LAPSER1 is a member of the LZTS family. Due to its deletion in multiple cancers, including prostate tumors, LAPSER1 is purported to be a tumor suppressor. In cancer cell lines, the overexpression of LAPSER1 can lead to growth inhibition and colony-forming efficiency. LAPSER1 is highly expressed in testis and prostate, but can be detected at lower levels in spleen, thymus, uterus, small intestine and colon. LAPSER1 colocalizes with ?tubulin, MKLP-1 and p80 katanin. LAPSER1 is involved in cytokinesis. The disruption of LAPSER1, which is accompanied by the mislocalization of p80 katanin, results in malformation of the central spindle. This is a potential impetus for carcinogenesis.

     

     

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