
Thermo Fisher Scientific Phospho-Huntington (Ser421) Polyclonal Antibody
인간 Huntington 단백질의 인산화된 Ser421 잔기를 특이적으로 인식하는 폴리클로날 항체입니다. Western blot, IHC, ELISA, IP 등 다양한 응용에 사용 가능하며, 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용됩니다.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500–1:2,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:100 |
| ELISA | 1:10,000–1:40,000 |
| Immunoprecipitation (IP) | 1:500–1:3,000 |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide corresponding to an internal region near aa 400–425 of human Huntington disease protein (pS421). Prepared from whole rabbit serum produced by repeated immunizations. |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.96 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | 0.02 M potassium phosphate, pH 7.2, with 0.15 M NaCl |
| Contains | 0.01% sodium azide |
| Storage Conditions | -20°C, avoid freeze/thaw cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
- Store vial at -20°C prior to opening.
- Aliquot contents and freeze at -20°C or below for extended storage.
- Avoid repeated freeze/thaw cycles.
- Centrifuge product if not completely clear after standing at room temperature.
- Stable for several weeks at 4°C as an undiluted liquid.
- Dilute only prior to immediate use.
This antibody is specific for phosphorylated human Huntington protein at the pS421 residue.
BLAST analysis indicates 100% homology of the immunizing sequence with Huntington homologues from chimpanzee, pig, and chicken.
Cross-reactivity with mouse and rat homologues may occur (one amino acid difference).
Minimal reactivity is expected with the non-phosphorylated form of the protein.
Target Information
Huntingtin is a disease gene linked to Huntington’s disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons. The disease is caused by an expanded trinucleotide repeat in the huntingtin gene, resulting in a polyglutamine repeat in the protein.
HD is an autosomal dominant disorder with mid-life onset, featuring psychiatric disorders, dementia, and involuntary movements (chorea), leading to death within 10–20 years.
The huntingtin locus spans 180 kb and consists of 67 exons. The gene is widely expressed and required for normal development.
It is expressed as two alternatively polyadenylated forms (~13.7 kb and ~10.3 kb) with different abundance in fetal and adult tissues.
The genetic defect may alter mRNA or protein function rather than eliminating transcription.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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