
Thermo Fisher Scientific ATXN7L1 Monoclonal Antibody (OTI4B12), TrueMAB
ATXN7L1 단백질을 인식하는 Mouse IgG1 단일클론 항체. Western blot에 최적화되어 있으며 Human 시료에 반응. 동결건조 형태로 제공되며, PBS buffer와 trehalose 포함. 연구용으로만 사용 가능.
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Applications
Western Blot (WB)
- Tested Dilution: 1:2,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI4B12 |
| Immunogen | Full length human recombinant protein of human ATXN7L1 produced in HEK293T cell |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage buffer | PBS, pH 7.3, with 8% trehalose |
| Contains | No preservative |
| Storage conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
For reconstitution, add 100 µL distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using this carrier-free antibody, perform an additional desalting step (Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).
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 encodes over 1,000 genes and constitutes about 5% of the human genome.
Mutations or deletions in this region have been linked to several genetic disorders, including osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia, and Shwachman-Diamond syndrome.
Deletion of part of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, characterized by mild intellectual disability, friendly demeanor, and distinctive facial features.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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