ATXN10 Antibody Blocking Peptide(bs-11806P)-500ug

ATXN10 Antibody Blocking Pepti

de(bs-11806P)-500ug
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  • ¥880
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  • bs-11806P
  • 2025年10月16日
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      500ug

    产品编号bs-11806P
    英文名称ATXN10 Antibody Blocking Peptide
    中文名称脊髓小脑共济失调10封闭多肽
    英文别名Ataxin 10; Ataxin-10; ATX10_HUMAN; Atxn10; Brain protein E46 homolog; E46L; FLJ37990; HUMEEP; Like mouse brain protein E46; SCA10; Spinocerebellar ataxia 10; Spinocerebellar ataxia type 10 protein.
    纯化方法HPLC
    研究领域

    Neuroscience > Neurology process > Neurogenesis

    亚基Homooligomer. Interacts with OGT. Interacts with GNB2. Interacts with IQCB1.
    亚细胞定位Cytoplasm, perinuclear region.
    组织特异性Expressed in the central nervous system.
    相似性Belongs to the ataxin-10 family.
    功能Necessary for the survival of cerebellar neurons. Induces neuritogenesis by activating the Ras-MAP kinase pathway. May play a role in the maintenance of a critical intracellular glycosylation level and homeostasis.
    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Spinocerebellar ataxia (SCA) is an autosomal dominant neurodegenerative disorder characterized by ataxia and selective neuronal cell loss. SCA is caused by the expansion of a translated CAG repeat, encoding a polyglutamine tract in SCA gene products, known as ataxins. The ataxin proteins are ubiquitously expressed in nervous tissue, but are primarily detected in cerebellum, brain stem and spinal cord in the central nervous system. Ataxin-10 is a cytoplasmic protein that belongs to the family of armadillo repeat proteins. A loss of ataxin-10 in primary neuronal cells causes increased apoptosis of cerebellar neurons. Ataxin-10 interacts with p110, an O-Linked beta-N-acetylglucosamine transferase, and may be important in the regulation of intracellular glycosylation levels and homeostasis in the brain. Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder that causes cerebellar ataxia and seizures. SCA10 is caused by an expansion of an ATTCT pentanucleotide repeat in intron 9 of the ataxin-10 gene.

     

     

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