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Thermo Fisher Scientific Ataxin 3 Recombinant Superclonal Antibody (13HCLC)
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Thermo Fisher Scientific Ataxin 3 Recombinant Superclonal Antibody (13HCLC)

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Recombinant Superclonal™ 항체로 높은 특이성과 재현성을 제공. 인간 Ataxin-3 단백질을 인식하며 WB, IHC, ICC/IF에 사용 가능. 폴리클로날 감도와 모노클로날 특이성을 결합한 고성능 항체. 연구용으로만 사용.

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pk
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Thermo Fisher Scientific 711823 Ataxin 3 Recombinant Superclonal Antibody (13HCLC) 100 ug pk판매 단위 pk
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Thermo Fisher Scientific · Thermo Fisher Scientific Ataxin 3 Recombinant Superclonal Antibody (13HCLC)

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 2.5 µg/mL View 1 publication
Immunohistochemistry (IHC) - View 1 publication
Immunocytochemistry (ICC/IF) 5 µg/mL -

Product Specifications

항목 내용
Species Reactivity Human
Published Species Mouse
Predicted Reactivity Monkey, Horse, Dog
Host / Isotype Rabbit / IgG
Expression System Expi293
Class Recombinant Superclonal
Type Antibody
Clone 13HCLC
Immunogen Protein corresponding to human Ataxin-3 (aa1–aa364)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7.4
Contains 0.09% sodium azide
Storage Conditions Store at 4°C short term; for long term, store at -20°C avoiding freeze/thaw cycles
Shipping Conditions Wet ice
RRID AB_2716916

Product Specific Information

Recombinant rabbit Superclonal™ antibodies are unique offerings from Thermo Fisher Scientific.
They combine multiple recombinant monoclonal antibodies to achieve both the sensitivity of polyclonal antibodies and the specificity of monoclonal antibodies, with the consistency of recombinant production.

  • Recognizes multiple epitope sites on the target
  • Provides higher detection sensitivity for low-abundance targets
  • Each lot is reproducible due to known light and heavy chain composition
  • Formerly called “Recombinant polyclonal antibody”, now rebranded as “Recombinant Superclonal™ antibody”
  • Physical product and performance remain unchanged

Target Information

Machado-Joseph disease (MJD), also known as spinocerebellar ataxia-3, is an autosomal dominant neurologic disorder.
The disease is caused by an expansion of (CAG)n repeats in the Ataxin-3 coding region (from normal 13–36 to 68–79 repeats).
There is a negative correlation between age of onset and CAG repeat number.

Ataxin-3 protein interacts with transcriptional regulators (CBP, p300, PCAF), represses transcription, and functions as a histone-binding deubiquitinating enzyme.


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

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