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Invitrogen™ Ataxin 2 Polyclonal Antibody
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Goat Polyclonal Antibody

Supplier:  Invitrogen™ PA5142597

Catalog No. PIPA5142597


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Description

Description

This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:2,000.

The autosomal dominant 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 dominant 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.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

Ataxin 2
Polyclonal
Unconjugated
Atxn2
9630045M23Rik; ASL13; ataxin 2; ataxin-2; ATX2; Atxn2; AW544490; FLJ46772; SCA2; spinocerebellar ataxia 2 (olivopontocerebellar ataxia 2, autosomal dominant, ataxin 2); spinocerebellar ataxia 2 homolog; spinocerebellar ataxia type 2 protein; Spinocerebellar ataxia type 2 protein homolog; TNRC13; Trinucleotide repeat-containing gene 13 protein
Goat
Ammonium sulfate precipitation
RUO
6311
-20°C, Avoid Freeze/Thaw Cycles
Liquid
Flow Cytometry, Immunocytochemistry
0.5 mg/mL
TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3
Q99700
Atxn2
Peptide with sequence C-SEREGHSINTR.
100 μg
Primary
Human
Antibody
IgG
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