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Thermo Fisher Scientific ATXN10 Polyclonal Antibody
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Thermo Fisher Scientific ATXN10 Polyclonal Antibody

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ATXN10 단백질을 인식하는 Thermo Fisher Scientific의 rabbit polyclonal antibody로, WB, IHC, ICC 등 다양한 응용에 사용 가능. 인간 시료 반응성이 높으며, 항원 친화 크로마토그래피로 정제됨. 연구용으로 단기 4°C, 장기 -20°C 보관 권장.

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마지막 업데이트 2025. 08. 05. 오전 02:59
Thermo Fisher Scientific PA561999 ATXN10 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific ATXN10 Polyclonal Antibody

Thermo Fisher Scientific ATXN10 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:500
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

Item Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human ATXN10. Recombinant protein control fragment (Product #RP-101275)
Conjugate Unconjugated
Form Liquid
Concentration 0.4 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_2638392

Product Specific Information

Immunogen sequence:
KHPESEWPFL IITDLFLKSP ELVQAMFPKL NNQERVTLLD LMIAKITSDE PLTKDDIPVF LRHAELIAST F

Highest antigen sequence identity to the following orthologs:

  • Mouse: 72%
  • Rat: 82%

Target Information

The autosomal dominant cerebellar ataxias (ADCAs) are a clinically and genetically heterogeneous group of disorders characterized by ataxia, dysarthria, dysmetria, and intention tremor. All ADCAs involve some degree of cerebellar dysfunction and varying degrees of signs from other components of the nervous system. A commonly accepted clinical classification (Harding, 1993) divides ADCAs into three different groups based on the presence or absence of associated symptoms such as brainstem signs or retinopathy.

  • ADCA I: presence of pyramidal and extrapyramidal symptoms and ophthalmoplegia
  • ADCA II: presence of retinopathy
  • ADCA III: absence of associated signs

Genetic linkage and molecular analyses revealed that ADCAs are genetically heterogeneous even within the various subtypes.

Additional Information

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

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