Thermo Fisher Scientific ATXN7L1 Polyclonal Antibody
ATXN7L1 단백질을 검출하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody입니다. Western blot과 IHC(Paraffin)에서 사용 가능하며, 인간·마우스·비인간 영장류에 반응합니다. 고순도 친화 크로마토그래피 정제, -20°C 보관.
- 카탈로그번호
- PA5114888
- 판매단위
- pk
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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, Non-human primate |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | A synthesized peptide derived from human ATXN7L1 (Accession Q9ULK2), corresponding to amino acid residues D96–V146 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage buffer | PBS with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage conditions | -20°C |
| Shipping conditions | Wet ice |
| RRID | AB_2899524 |
Product Specific Information
Antibody detects endogenous levels of total ATXN7L1.
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 (~158 million bases) encodes over 1,000 genes and comprises about 5% of the human genome.
Chromosome 7 has been linked to disorders such as 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, sociable behavior, and distinctive facial features.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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