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Ataxin-7 Polyclonal Antibody, Bethyl Laboratories

Rabbit Polyclonal Antibody

Supplier:  Bethyl Laboratories, Inc A302638AT

Encompass_Preferred

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Catalog No. 50-156-3092


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Description

Description

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

Spinocerebellar ataxia type 7 (SCA7) belongs to a class of hereditary neurodegenrative diseases characterized by abnormally expanded polyglutamine (CAG) repeats at the N-terminus. This autosomal domit cerebellar ataxia primarily affects the cerebellum, retina, and brain stem and causes dementia, macular degeneration and other neurodegenerative characteristics. SCA7 gene encodes the ubiquitous 892 residue protein ataxin-7. This protein is typically located in the cytoplasm and on the nuclear membrane of normal brain neurons. In cells where there is a mutation of the SCA7 gene, ataxin 7 accumulates in intranuclear inclusions and can result in cell death.
Specifications

Specifications

Ataxin-7
Polyclonal
TBS with 0.1% BSA and 0.09% sodium azide
O15265
ATXN7
Between 842 and 892
20 μL
Primary
Human
Antibody
IgG
Western Blot
Unconjugated
ATXN7
ADCAII, OPCA3, SCA7
Rabbit
Antigen affinity chromatography
RUO
6314
4° C
Liquid
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