Ataxin 1 Antibody

Defects in Ataxin-1 are the cause of spinocerebellar ataxia type 1 (SCA1), also known as olivopontocerebellar atrophy I (OPCA I or OPCA1). Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to cerebellum degeneration with variable involvement of the brainstem and spinal cord. SCA1 is caused by expansion of a CAG repeat in the coding region of the ataxin-1 gene. Longer expansions result in earlier onset and more severe clinical manifestations of the disease. Ataxin-1 binds RNA in vitro and may be involved in RNA metabolism. [Uniprot]

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Showing Publication 1 - 1 of 1.

Publication using NBP1-45237	Applications	Species
Banfi S, Servadio A, Chung MY et al. Identification and characterization of the gene causing type 1 spinocerebellar ataxia Nat Genet 1994-08-01 [PMID: 7951322]

Array NBP1-45237

• Ataxin 1 Antibodies
• Ataxin 1 ELISA Kits
• Ataxin 1 Lysates
• Ataxin 1 Proteins