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Invitrogen™ Ataxin 7 Monoclonal Antibody (3SCA-1C1)

Mouse Monoclonal Antibody

Supplier:  Invitrogen™ MA3083

Catalog No. PIMA3083


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Description

Description

MA3-083 detects Ataxin 7 from human and mouse samples. MA3-083 has been successfully used in Western blot, immunofluorescence, and ELISA applications. The MA3-083 epitope is mapped between aa 66 and aa 119.

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.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

Ataxin 7
Monoclonal
Conc. Not Determined
Ascites with 0.05% sodium azide
O15265, Q8R4I1
ATXN7
Recombinant human Ataxin 7 aa 1 - 229.
RUO
246103, 6314
-20°C, Avoid Freeze/Thaw Cycles
Liquid
Western Blot, Immunocytochemistry
3SCA-1C1
Unconjugated
ATXN7
A430107N12Rik; ADCAII; AI627028; Ataxin 7; Ataxin7; Ataxin-7; ATXN7; Atxn7-PA; Atxn7-PB; Atxn7-PC; Atxn7-PD; CG9866; CG9866-PA; CG9866-PB; CG9866-PC; CG9866-PD; Dmel\CG9866; Dmel_CG9866; LD40170p; OPCA3; RGD1562692; SCA7; spinocerebellar ataxia 7 homolog; spinocerebellar ataxia type 7 protein; Spinocerebellar ataxia type 7 protein homolog
Mouse
50 μL
Primary
Human, Mouse
Antibody
IgG1 κ
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