
Thermo Fisher Scientific Phospho-Huntington (Ser421) Polyclonal Antibody
Huntington 단백질의 Ser421 인산화 형태를 인식하는 폴리클로날 항체. Western blot, IHC, ELISA, IP 등 다양한 어플리케이션에 사용 가능. 인간, 생쥐, 랫트 반응성. -20°C 보관, 동결-해동 반복 피해야 함. 연구용 전용.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:2,000 |
| Immunohistochemistry (IHC) | Assay-dependent |
| ELISA | 1:10,000 |
| Immunoprecipitation (IP) | 1 µg/mL |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Anti-Huntington pS421 affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to the internal region of human Huntington disease protein. |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | 0.02M potassium phosphate, pH 7.2, with 50% glycerol, 0.15M NaCl |
| Contains | No preservative |
| 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 cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4°C as an undiluted liquid. Dilute only prior to immediate use.
Anti-Huntingtin pS421 is directed against the phosphorylated form of the S421 residue. A BLAST analysis suggests cross-reactivity with human based on 100% sequence homology. Cross-reactivity with Huntington pS421 from other sources has not been determined.
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 huntingtin gene is widely expressed and is required for normal development. It is expressed as two alternatively polyadenylated forms with different relative abundance in various fetal and adult tissues. The larger transcript (~13.7 kb) is expressed predominantly in adult and fetal brain, while the smaller transcript (~10.3 kb) is more widely expressed.
The genetic defect leading to Huntington’s disease may not eliminate transcription but may confer a new property on the mRNA or alter the function of the protein.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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