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Thermo Fisher Scientific Huntingtin Recombinant Superclonal Antibody (3HCLC)
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Thermo Fisher Scientific Huntingtin Recombinant Superclonal Antibody (3HCLC)

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Huntingtin 단백질을 인식하는 Thermo Fisher의 Recombinant Superclonal™ 항체로, 인간 및 예측된 원숭이·생쥐·소 반응성. 높은 감도와 재현성을 제공하며, 단일 클론과 다클론의 장점을 결합한 구조. 연구용으로만 사용 가능.

카탈로그번호
710695
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 07:19
Thermo Fisher Scientific 710695 Huntingtin Recombinant Superclonal Antibody (3HCLC) 100 ug pk판매 단위 pk ·
재고 확인 필요
614,900원VAT 포함 676,390원

Thermo Fisher Scientific · Thermo Fisher Scientific Huntingtin Recombinant Superclonal Antibody (3HCLC)

Applications

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System Expi293
Class Recombinant Superclonal
Type Antibody
Clone 3HCLC
Immunogen Peptides corresponding to Human HTT (aa 82–99, 584–601, 650–666)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7.2
Contains 0.09% 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_2608784

Product Specific Information

  • Predicted to react with Monkey, Mouse, and Bovine.
  • Recombinant rabbit Superclonal™ antibodies combine multiple recombinant monoclonal antibodies, offering polyclonal sensitivity with monoclonal specificity and recombinant consistency.
  • Each lot is produced with a known mixture of light and heavy chains, avoiding biological variability of polyclonal antibodies.
  • Formerly called “Recombinant polyclonal antibody”, now rebranded as “Recombinant Superclonal™ antibody”.
  • Physical product and performance remain unchanged.

Target Information

Huntingtin is a disease gene linked to Huntington’s disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons. The disorder is caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product.
HD is a mid-life onset autosomal dominant neurodegenerative disease characterized by psychiatric disorders, dementia, and involuntary movements (chorea), leading to death in 10–20 years.
The huntingtin locus spans 180 kb and consists of 67 exons. It is widely expressed and required for normal development, with two alternatively polyadenylated forms showing different abundance in fetal and adult tissues.
The larger transcript (~13.7 kb) is mainly expressed in brain, while the smaller (~10.3 kb) is more broadly expressed.
The genetic defect may not eliminate transcription but can alter mRNA or protein function.


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

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