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Ataxin-7 Polyclonal Antibody, Bethyl Laboratories
Rabbit Polyclonal Antibody
Supplier: Bethyl Laboratories, Inc A302638AT

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
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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