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Thermo Fisher Scientific Huntingtin Recombinant Rabbit Monoclonal Antibody (3H2L4)
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Thermo Fisher Scientific Huntingtin Recombinant Rabbit Monoclonal Antibody (3H2L4)

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Huntingtin 단백질을 인식하는 재조합 토끼 단클론 항체로, ICC/IF에 적합합니다. Expi293 시스템에서 발현되며 로트 간 일관성과 높은 특이성을 제공합니다. 인간, 원숭이, 생쥐, 소 시료에 반응 예측됩니다. 연구용으로만 사용 가능합니다.

카탈로그번호
701663
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오후 11:18
Thermo Fisher Scientific 701663 Huntingtin Recombinant Rabbit Monoclonal Antibody (3H2L4) 100 ug pk판매 단위 pk ·
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691,200원VAT 포함 760,320원

Thermo Fisher Scientific · Thermo Fisher Scientific Huntingtin Recombinant Rabbit Monoclonal Antibody (3H2L4)

Applications

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 5 µg/mL

Product Specifications

항목 내용
Host / Isotype Rabbit / IgG
Expression System Expi293
Class Recombinant Monoclonal
Type Antibody
Clone 3H2L4
Immunogen Peptides corresponding to Human HTT (aa 584–601, 650–666, 82–99)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
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_2633029

Product Specific Information

This antibody is predicted to react with Monkey, Mouse, and Bovine.

Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems. These systems clone specific antibody DNA sequences from immunoreactive rabbits. Individual clones are screened to select the best candidates for production.

Advantages:

  • High specificity and sensitivity
  • Lot-to-lot consistency
  • Animal origin-free formulation
  • Broader immunoreactivity due to larger rabbit immune repertoire

Target Information

Huntingtin is a disease gene linked to Huntington’s disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons. This is caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, translating as a polyglutamine repeat in the protein product.

HD typically manifests in mid-life as an autosomal dominant neurodegenerative disease characterized by psychiatric disorders, dementia, and involuntary movements (chorea), leading to death within 10–20 years.

The huntingtin locus spans approximately 180 kb and consists of 67 exons. It is widely expressed and required for normal development. Two alternatively polyadenylated forms exist, showing different abundance in fetal and adult tissues. The larger transcript (~13.7 kb) is predominant in brain, while the smaller (~10.3 kb) is more broadly expressed.

The genetic defect leading to Huntington’s disease may not eliminate transcription but may alter mRNA properties or protein function.


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

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