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      Ó¢ÎÄÃû³Æ£º ATXN1 Antigen (Recombinant Protein)

      ±ð      Ãû£º ATX1; SCA1; D6S504E

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


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      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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