Thermo Fisher Scientific FAM111B Polyclonal Antibody
FAM111B 단백질을 인식하는 Rabbit Polyclonal 항체로 Western Blot에 최적화됨. Human, Mouse, Rat에 반응하며 항원 친화 크로마토그래피로 정제됨. 고순도(>95%) 항체로 연구용에 적합하며 PBS/glycerol buffer로 안정화되어 장기 보관 가능.
- 판매단위
- pk
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Applications
- Western Blot (WB): 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 FAM111B |
| 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_2719578 |
Product Specific Information
The antibody was affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.
Target Information
FAM111B is a 734 amino acid protein encoded by a gene located on human chromosome 11, which constitutes about 4% of human genomic DNA. Chromosome 11 contains numerous genes associated with various diseases. The ATM gene on chromosome 11 regulates cell cycle arrest and apoptosis following DNA double-strand breaks, and its mutation causes ataxia-telangiectasia. Mutations in HBB lead to sickle cell anemia and beta thalassemia. WT1 gene mutations are linked to Wilms’ tumor, WAGR syndrome, and Denys-Drash syndrome. Additionally, defects in chromosome 11 are associated with Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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