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Thermo Fisher Scientific HD Monoclonal Antibody (3F9)
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Thermo Fisher Scientific HD Monoclonal Antibody (3F9)

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Huntingtin 단백질을 인식하는 3F9 클론의 마우스 단클론 항체. Western blot과 ELISA에 최적화되어 있으며, 친화 크로마토그래피로 정제된 액상 형태. 인간 시료 반응성, 보존제 무첨가, -20°C 보관.

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pk
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마지막 업데이트 2025. 08. 05. 오후 04:05
Thermo Fisher Scientific H00003064-M06 HD Monoclonal Antibody (3F9) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific HD Monoclonal Antibody (3F9)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–5 µg/mL
ELISA 0.3 ng/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone 3F9
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Immunogen

HD (NP_002102, 81 a.a. approximately 190 a.a) partial recombinant protein with GST tag.
Molecular weight of GST tag alone: 26 kDa.

Target Family: Huntingtin
UniProt ID: P42858-1
Species: Human (NCBI Node ID: 9606)
Antigen Range: 81–190

Product Specific Information

Protein Sequence:
AVAEEPLHRP KKELSATKKD RVNHCLTICE NIVAQSVRNS PEFQKLLGIA MELFLLCSDD AESDVRMVAD ECLNKVIKAL MDSNLPRLQL ELYKEIKKNG APRSLRAALW

Target Information

Huntingtin is a disease gene linked to Huntington’s disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be 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. The gene is widely expressed and required for normal development. Two alternatively polyadenylated forms are expressed with different abundance in fetal and adult tissues.
The larger transcript (~13.7 kb) is mainly in brain tissue, while the smaller (~10.3 kb) is expressed more broadly. The genetic defect may not eliminate transcription but may 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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