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ATX2/SCA2 Polyclonal Antibody, Bethyl Laboratories

Catalog No. 501559304
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50-155-9304 20 μL
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Catalog No. 50-155-9304 Supplier Bethyl Laboratories, Inc Supplier No. A301118AT
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Rabbit Polyclonal Antibody

The recommended shelf life for this product is 1 year from date of receipt.

The autosomal domit 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. Defects in this gene are the cause of spinocerebellar ataxia type 2 (SCA2). SCA2 belongs to the autosomal domit cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. SCA2 is caused by expansion of a CAG repeat in the coding region of this gene. Longer expansions result in earlier onset of the disease. Alternatively spliced transcript variants encoding different isoforms have been identified but their full length sequence has not been determined.

Specifications

Antigen ATX2/SCA2
Applications Western Blot
Classification Polyclonal
Conjugate Unconjugated
Formulation TBS with 0.1% BSA and 0.09% sodium azide
Gene ATXN2
Gene Accession No. O70305, Q99700
Gene Alias TNRC13, ATX2, SCA2, ataxin 2, ASL13, ATXN2
Gene Symbols Atxn2
Host Species Rabbit
Immunogen Between 1262 and 1312
Purification Method Antigen affinity chromatography
Quantity 20 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 20239, 6311
Target Species Human, Mouse
Content And Storage 4° C
Product Type Antibody
Form Liquid
Isotype IgG
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