Thermo Fisher Scientific ATXN7L1 Polyclonal Antibody
ATXN7L1 단백질을 인식하는 Thermo Fisher Scientific의 고순도 폴리클로날 항체입니다. Western blot 검증 완료. 인간, 마우스, 랫트 반응성. 항원 친화 크로마토그래피 정제. 연구용으로만 사용 가능.
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Thermo Fisher Scientific ATXN7L1 Polyclonal Antibody
Applications
- Western Blot (WB)
Tested Dilution: 1:500–1:1,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide corresponding to residues in Human ATXN7L1 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS, pH 7.2, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2719599 |
Product Specific Information
The antibody was affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen.
Purity is >95% (by SDS-PAGE).
Target Information
ATXN7L1 (ataxin-7-like protein 1) is an 833 amino acid protein containing one SCA7 domain.
The ATXN7L1 gene is conserved in chimpanzee, canine, mouse, rat, and chicken, and maps to human chromosome 7q22.3.
Chromosome 7, approximately 158 million bases long, encodes over 1,000 genes and constitutes about 5% of the human genome.
It 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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