FAM193B Antibody Blocking Peptide(bs-14772P)-500ug产品图

FAM193B Antibody Blocking Pept

ide(bs-14772P)-500ug
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  • ¥880
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  • bs-14772P
  • 2025年10月16日
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      500ug

    产品编号bs-14772P
    英文名称FAM193B Antibody Blocking Peptide
    中文名称FAM193B蛋白封闭多肽
    英文别名Family with sequence similarity 193, member B; IRIZIO; F193B_HUMAN; Protein FAM193B.
    纯化方法HPLC
    相似性Belongs to the FAM193 family.
    功能FAM193B, also known as IRIZIO, was initially identified as a protein that is upregulated in alveolar rhabdomyosarcoma (ARMS), a type of fast-growing tumor characterized by chromosomal translocations fusing the PAX3 or PAX7 gene with that of FOXO1. It has been suggested that, in addition to the PAX3-FOXO1 gene fusion, disruption of the Rb and p53 pathways is required for full ARMS tumorigenesis. In PAX3-FOXO1-expressing primary mouse fibroblasts that possessed a defective p53 pathway, FAM193B expression enabled the tumorigenic transformation, suggesting that FAM193B may contribute to rhabdomyosarcomagenesis in humans.
    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FAM193B is a 902 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding FAM193B maps to human chromosome 5, which contains 181 million base pairs and encodes around 1,000 genes. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

     

     

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