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Thermo Fisher Scientific Ataxin 1 Monoclonal Antibody (N76/8), PerCP
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Thermo Fisher Scientific Ataxin 1 Monoclonal Antibody (N76/8), PerCP

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Ataxin 1 단백질을 검출하기 위한 PerCP 결합 단클론 항체로, Western blot, IHC, ICC/IF, IP 등에 사용 가능. 인간, 생쥐, 랫드 반응성. 단일 클론 N76/8, Protein G 정제, 4°C 보관. 연구용 전용 제품.

카탈로그번호
MA545664
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 06:18
Thermo Fisher Scientific MA545664 Ataxin 1 Monoclonal Antibody (N76/8), PerCP 100 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

Thermo Fisher Scientific · Thermo Fisher Scientific Ataxin 1 Monoclonal Antibody (N76/8), PerCP

Applications and Tested Dilutions

Application Tested Dilution Notes
Western Blot (WB) 1:1,000
Immunohistochemistry (IHC) Assay-dependent
Immunocytochemistry (ICC/IF) 1:100
Immunoprecipitation (IP) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone N76/8
Immunogen Synthetic peptide (aa 164–197: ATTPSQRSQLEAYSTLLANMGSLSQAPGHKVEPP) of mouse Ataxin-1
Conjugate PerCP
Excitation / Emission Max 482 / 675 nm
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer 95.64 mM phosphate / 2.48 mM MES, pH 7.4, with 0.5 M EDTA
Contains No preservative
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2932118

Additional Formats Available:


Product Specific Information

  • Rat: 100% identity (34/34 amino acids identical)
  • Human: 88% identity (30/34 amino acids identical)
  • 1 µg/mL of MA5-45664 detects Ataxin-1 in 20 µg of rat brain lysate by colorimetric immunoblot using Goat anti-mouse IgG:HRP as secondary antibody.
  • Detects approximately 85 kDa protein.
  • Formerly sold as clone S76-8.

Target Information

Autosomal dominant cerebellar ataxias (ADCA) are heterogeneous neurodegenerative disorders involving progressive degeneration of the cerebellum, brain stem, and spinal cord.
ADCA is divided into three groups (types I–III).
Type I includes spinocerebellar ataxia (SCA) 1, 2, 3, 4, and 6.
Type II (SCA7) presents with retinal degeneration, and Type III (SCA5) is a pure cerebellar syndrome.
These diseases result from CAG repeat expansions in coding regions, leading to elongated polyglutamine tracts.
The Ataxin 1 gene, mapped to chromosome 6, is associated with spinocerebellar ataxia type 1 (SCA1).
Disease alleles contain 41–81 CAG repeats compared to 6–39 in normal alleles.
At least two transcript variants encoding the same protein have been identified.


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


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