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Ataxin 7 Rabbit anti-Human, Polyclonal, Bioss
SDP

Catalog No. 501981263
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50-198-1263 100 μL
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Catalog No. 50-198-1263 Supplier Bioss Supplier No. BS11318R
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Rabbit Polyclonal Antibody

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 dominant 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

Antigen Ataxin 7
Applications Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 1 μg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Gene ATXN7
Gene Accession No. O15265
Gene Alias A430107N12Rik; ADCAII; AI627028; ataxin 7; Ataxin-7; Atxn7; Atxn7-PA; Atxn7-PB; Atxn7-PC; Atxn7-PD; CG9866; CG9866 gene product from transcript CG9866-RA; CG9866-PA; CG9866-PB; CG9866-PC; CG9866-PD; Dmel\CG9866; Dmel_CG9866; OPCA3; RGD1562692; SCA7; spinocerebellar ataxia 7 homolog; Spinocerebellar ataxia type 7 protein; Spinocerebellar ataxia type 7 protein homolog
Gene Symbols ATXN7
Host Species Rabbit
Immunogen KLH conjugated synthetic peptide derived from human Ataxin 7.
Purification Method Protein A
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 6314
Target Species Human
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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