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TCF25 Antibody Blocking Peptid

e(bs-9604P)-500ug
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  • 2025年10月16日
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      500ug

    产品编号bs-9604P
    英文名称TCF25 Antibody Blocking Peptide
    中文名称核转录因子25封闭多肽
    英文别名FKSG26; hKIAA1049; NULP1; PRO2620; Hulp1; KIAA1049; Nuclear localized protein 1; Transcription factor 25 (basic helix loop helix); TCF25_HUMAN.
    纯化方法HPLC
    研究领域

    Cardiovascular > Heart > Cardiogenesis > Transcription factors/regulators

    Epigenetics and Nuclear Signaling > Transcription > Polymerase associated factors > Pol II Transcription

    亚基Interacts with XIAP (By similarity).
    亚细胞定位Nuclear. Note=Some staining in the cytosol.
    组织特异性In the embryo, widely expressed with highest levels in brain. In the adult, highest expression is found in the heart.
    相似性Belongs to the TCF25 family.
    功能May play a role in cell death control. Acts as a transcriptional repressor. Has been shown to repress transcription of SRF in vitro and so may play a role in heart development.
    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Transcription factor 25 acts as a transcriptional repressor. It has been shown to repress transcription of SRF in vitro and hence may play a role in heart development.Transcription factor 25, is a 676 amino acid protein that plays a role in cell death. A member of the TCF25 family, Nulp1 utilizes its C-terminus to mediate transcriptional repression of SRF in vitro, and interacts with XIAP. Nulp1 localizes primarily to the nucleus but is also found in cytosol. Widely expressed, Nulp1 is found at high levels in embryonic brain and adult heart. The gene encoding Nulp1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

     

     

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