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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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Ataxin 2 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal 항체. WB 및 IHC에 사용 가능하며 Human, Mouse, Rat 반응성. 합성 펩타이드 항원을 이용해 제작된 비결합 항체로, 신경퇴행성 질환 연구에 적합.

카탈로그번호
OSA00181W-100UL
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 04:33
Thermo Fisher Scientific OSA00181W-100UL Ataxin 2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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542,600원VAT 포함 596,860원

Thermo Fisher Scientific · Thermo Fisher Scientific Ataxin 2 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:300–1:2,000 -
Immunohistochemistry (IHC) 1:300–1:2,000 -
Miscellaneous PubMed (Misc) - View 3 publications

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from amino acid region 900–1000 of mouse Ataxin 2 conjugated to an immunogenic carrier protein
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Storage Buffer Whole serum
Contains No preservative
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. Glycerol (1:1) may be added for added stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Reconstitute in 100 µL of sterile water.
  • Centrifuge to remove any insoluble material.
  • Specificity: Ataxin-2.

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. Clinically, ADCA has been divided into three groups: ADCA types I–III.
Defects in this gene cause spinocerebellar ataxia type 2 (SCA2), belonging to ADCA type I, characterized by cerebellar ataxia with 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 lead to earlier disease onset. Alternatively spliced transcript variants encoding different isoforms have been identified, but 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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