
Thermo Fisher Scientific HD Monoclonal Antibody (3F9)
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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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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