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Thermo Fisher Scientific Ataxin 1 Polyclonal Antibody
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Thermo Fisher Scientific Ataxin 1 Polyclonal Antibody

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Ataxin 1 단백질을 인식하는 Rabbit Polyclonal 항체로, WB, IHC, ICC, Flow Cytometry에 적합합니다. Human, Mouse, Rat에 반응하며, 항원 친화 크로마토그래피로 정제되었습니다. 동결건조 형태로 제공되며, 재구성 시 500 µg/mL 농도로 사용 가능합니다.

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마지막 업데이트 2025. 08. 03. 오후 10:42
Thermo Fisher Scientific PA578844 Ataxin 1 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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568,000원VAT 포함 624,800원

Thermo Fisher Scientific · Thermo Fisher Scientific Ataxin 1 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 0.1–0.5 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 0.5–1 µg/mL
Immunocytochemistry (ICC/IF) 5 µg/mL
Flow Cytometry (Flow) 1–3 µg/1×10⁶ cells

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide corresponding to a sequence at the C-terminus of human Ataxin 1 (778–808aa ESRKLEKSEDEPPLTLPKPSLIPQEVKICIE)
Conjugate Unconjugated
Form Lyophilized
Concentration 500 µg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with 5 mg BSA
Contains 0.05 mg sodium azide
Storage Conditions -20°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2745960

Product Specific Information

Reconstitute with 0.2 mL of distilled water to yield a concentration of 500 µg/mL.

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 is divided into three groups (types I–III). ADCAI is genetically heterogeneous, involving loci SCA1, 2, 3, 4, and 6. ADCAII (SCA7) presents with retinal degeneration, while ADCAIII (SCA5) is often referred to as the “pure” cerebellar syndrome. These disorders are caused by expansion of CAG repeats, producing elongated polyglutamine tracts in the corresponding proteins. The Ataxin 1 gene is mapped to chromosome 6, with diseased alleles containing 41–81 CAG repeats (normal: 6–39), associated with spinocerebellar ataxia type 1 (SCA1). 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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