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IWS1 Antibody Blocking Peptide

(bs-17190P)-500ug
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  • ¥880
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  • bs-17190P
  • 2025年10月16日
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      500ug

    产品编号bs-17190P
    英文名称IWS1 Antibody Blocking Peptide
    中文名称IWS1蛋白封闭多肽
    英文别名DKFZp761G0123; FLJ10006; FLJ14655; FLJ32319; Interacts with Spt6; iws1; IWS1 homolog; IWS1-like protein; IWS1_HUMAN; IWS1L; MGC126375; MGC126376; OTTHUMP00000162262; Protein IWS1 homolog.
    纯化方法HPLC
    研究领域

    Epigenetics and Nuclear Signaling > DNA / RNA > RNA Processing > Splicing

    亚基Interacts with SUPT6H; binds preferentially to the POLR2A-bound SUPT6H. Interacts with ALYREF/THOC4, SETD2 and PRMT5. Interacts with HDGFRP2.
    亚细胞定位Nucleus.
    相似性Belongs to the IWS1 family.
    Contains 1 TFIIS N-terminal domain.
    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HIws1 is an 819 amino acid nuclear protein that contains one TFIIS N-terminal domain. Belonging to the IWS1 family, hIws1 exists as three alternatively spliced isoforms, which are encoded by a gene mapping to human chromosome 2q14.3. Chromosome 2 is the second largest human chromosome, consisting of 237 million bases, encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome, is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes

     

     

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