Thermo Fisher Scientific ATXN7L1 Polyclonal Antibody
ATXN7L1 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot 및 IHC(Paraffin) 응용에 적합하며, 인간·마우스·랫트 반응성. 고순도 친화 크로마토그래피 정제, -20°C 보관.
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Applications
Western Blot (WB)
- Tested Dilution: 1:1,000–1:3,000
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:50–1:200
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | A synthesized peptide derived from human ATXN7L1 (Accession Q9ULK2), corresponding to amino acid residues R476–P526 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.4, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C |
| Shipping Conditions | Wet ice |
| RRID | AB_2852959 |
Product Specific Information
Antibody detects endogenous levels of total ATXN7L1.
Target Information
ATXN7L1 (ataxin-7-like protein 1) is an 833 amino acid protein that contains one SCA7 domain.
The ATXN7L1 gene is conserved in chimpanzee, canine, mouse, rat, and chicken, and maps to human chromosome 7q22.3.
Chromosome 7 is about 158 million bases long, encodes over 1,000 genes, and makes up about 5% of the human genome.
Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia, and Shwachman-Diamond syndrome.
Deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, characterized by mild mental retardation, friendliness with strangers, and an elfin appearance.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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