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| Antigenic Specificity | ATX2/SCA2 |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | human, mouse |
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| Isotype | n/a |
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| Format | purified |
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| Size | 100 µL |
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| Concentration | n/a |
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| Applications | Immunoprecipitation: 2-5 µg/mg lysate, Western Blot: 1:1,000-1:5,000 |
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| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
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| Description | ATX2/SCA2 Polyclonal Antibody. 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 |
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| Immunogen | n/a |
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| Other Names | TNRC13, ATX2, SCA2, ataxin 2, ASL13, ATXN2 |
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| Gene, Accession # | Entrez: 20239, 6311; Uniprot: O70305, Q99700 |
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| Catalog # | A301-118A |
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| Price | |
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| Order / More Info | ATX2/SCA2 Antibody from INVITROGEN ANTIBODIES |
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| Product Specific References | n/a |
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