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    • ATXN1抗原(重組蛋白)

      規(guī)格:
      價(jià)格:
      • 品牌 : 通蔚生物
      • 目錄號(hào) : TW16792
      • 應(yīng)用 : 僅供科研使用
      • 貨期 : 現(xiàn)貨
      • 規(guī)格 :1mg/100ug
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    中文名稱:ATXN1抗原(重組蛋白)

    英文名稱: ATXN1 Antigen (Recombinant Protein)

    別      名: ATX1; SCA1; D6S504E

    儲(chǔ)      存: 冷凍(-20℃)

    相關(guān)類別: 抗原

    概  述:

    Fusion protein corresponding to C terminal 270 amino acids of human ATXN1


    技術(shù)規(guī)格:

    Full name:

    ataxin 1

    Synonyms:

    ATX1; SCA1; D6S504E

    Swissprot:

    P54253

    Gene Accession:

    BC117125

    Purity:

    >85%, as determined by Coomassie blue stained SDS-PAGE

    Expression system:

    Escherichia coli

    Tags:

    His tag C-Terminus, GST tag N-Terminus

    Background:

    The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions.


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