FAM126A Antibody Blocking Peptide(bs-11554P)-500ug

FAM126A Antibody Blocking Pept

ide(bs-11554P)-500ug
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  • ¥880
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  • bs-11554P
  • 2025年10月16日
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      500ug

    产品编号bs-11554P
    英文名称FAM126A Antibody Blocking Peptide
    中文名称髓鞘缺陷相关蛋白封闭多肽
    英文别名Hyccin; Down regulated by Ctnnb1 a; Down regulated by CTNNB1 protein A; Down-regulated by CTNNB1 protein A; DRCTNNB1A; FAM126A; Family with sequence similarity 126 member A; HCC; HLD5; HYCC1; HYCCI_HUMAN antibody Hyccin; Protein FAM126A.
    纯化方法HPLC
    研究领域

    Developmental Biology > Organogenesis > Nervous system development

    Neuroscience > Neurology process > Neural Signal Transduction

    Neuroscience > Neurology process > Neurogenesis

    亚细胞定位Cytoplasm. Membrane. According to PubMed:10910037, it is mainly cytoplasmic while according to PubMed:16951682, it is a membrane protein.
    组织特异性Widely expressed. Highest levels in heart, brain, placenta, spleen and testis.
    相似性Belongs to the FAM126 family.
    功能May have a role in the beta-catenin/Lef signaling pathway. May have a role in the process of myelination of the central and peripheral nervous system.
    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Hyccin is a 521 amino acid cytoplasmic protein that is widely expressed with highest levels found in heart, brain, placenta, spleen and testis. Belonging to the FAM126 family, hyccin may play a role in the ∫-catenin/Lef signaling pathway. Hyccin is likely involved in the process of myelination of the central and peripheral nervous system. Defects in the gene encoding hyccin are the cause of leukodystrophy hypomyelinating type 5 (HLD5), which is characterized by congenital cataract, progressive neurologic impairment and diffuse myelin deficiency. Individuals affected by HLD5 experience progressive pyramidal and cerebellar dysfunction along with muscle weakness in the lower limbs. Hyccin exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 7.

     

     

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