STIL Antibody Blocking Peptide(bs-9303P)-500ug

STIL Antibody Blocking Peptide

(bs-9303P)-500ug
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  • ¥880
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  • bs-9303P
  • 2025年10月16日
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      500ug

    产品编号bs-9303P
    英文名称STIL Antibody Blocking Peptide
    中文名称中断位点蛋白STIL封闭多肽
    英文别名MCPH7; SCL interrupting locus protein; SCL-interrupting locus protein; SCL/TAL1 interrupting locus; SIL; STIL; STIL_HUMAN; TAL 1 interrupting locus protein; TAL-1-interrupting locus protein.
    纯化方法HPLC
    研究领域

    Cell Biology > Cell Cycle > Cell Division > Other cell division antibodies

    Stem Cells > Signaling Pathways > Hedgehog > Cytoplasmic

    亚基Interacts with PIN1 via its WW domain. This interaction is dependent on STIL mitotic phosphorylation (By similarity).
    亚细胞定位Cytoplasm, cytosol.
    组织特异性Expressed in all hematopoietic tissues and cell lines. Highly expressed in a variety of tumors characterized by increased mitotic activity with highest expression in lung cancer.
    翻译后修饰Phosphorylated following the activation of the mitotic checkpoint.
    功能Immediate-early gene. Plays an important role in embryonic development as well as in cellular growth and proliferation; its long-term silencing affects cell survival and cell cycle distribution as well as decreases CDK1 activity correlated with reduced phosphorylation of CDK1. Plays a role as a positive regulator of the sonic hedgehog pathway, acting downstream of PTCH1.
    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TAL1 disruption at 1p32, a common rearrangement in the T-cell acute lymphoblastic leukemia, usually results in the formation of a SCL interrupting locus (SIL)-TAL1 fusion product. SIL is an immediate early gene whose expression is associated with cell proliferation. The Sil protein exhibits ubiquitous expression in hematopoietic cell lines and tissues. However, Sil protein levels remain tightly regulated during the cell cycle, achieving peak levels in mitosis and diminishing on transition to G1 phase. Overexpression of Sil in primary adenocarcinomas predicts metastatic spread, especially in lung tumors with increased mitotic activity.

     

     

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