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Thermo Fisher Scientific Ataxin 2 Polyclonal Antibody
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Thermo Fisher Scientific Ataxin 2 Polyclonal Antibody

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Human Ataxin 2 단백질을 인식하는 Rabbit Polyclonal Antibody로, WB, IHC, ICC, IP 등 다양한 응용에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며 PBS/glycerol buffer에 보관. 신경퇴행성 질환 연구용으로 적합.

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마지막 업데이트 2025. 08. 04. 오후 12:52
Thermo Fisher Scientific PA554183 Ataxin 2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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796,700원VAT 포함 876,370원

Thermo Fisher Scientific · Thermo Fisher Scientific Ataxin 2 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:500
Immunocytochemistry (ICC/IF) Assay-dependent
Immunoprecipitation (IP) Assay-dependent

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human Ataxin 2. Recombinant protein control fragment (Product #RP-91710).
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2638321

Product Specific Information

Immunogen sequence:
EGHSINTREN KYIPPGQRNR EVISWGSGRQ NSPRMGQPGS GSMPSRSTSH TSDFNPNSGS DQRVVNGGVP WPSPCPSPSS RPPSRYQSGP NSLPPRAATP TRPPSRPPSR PSRPPSHPSA HGSPAPVSTM PKRMSSE

Highest antigen sequence identity to orthologs:

  • Mouse: 93%
  • Rat: 95%

Target Information

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. ADCA has been divided into three groups: types I–III.
Defects in this gene cause spinocerebellar ataxia type 2 (SCA2), belonging to ADCA type I, characterized by cerebellar ataxia with additional clinical features such as optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy, and dementia.
SCA2 results from expansion of a CAG repeat in the coding region of this gene, where longer expansions lead to earlier disease onset. Alternatively spliced transcript variants encoding different isoforms have been identified, though their full-length sequences have not been determined.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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