- W16207A (See other available formats)
- Other Names
- F-box only protein 7
- Rat IgG2a, κ
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- Product Citations
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F-box only protein 7 (FBXO7) is involved in the ubiquitination process during protein degradation. FBXO7 is a subunit of the SCF (SKP1/cullin‐1/F‐box protein) complex. The scaffold proteins cullin‐1 and SKP1, the RING subunit Rbx1 together with the substrate‐recruiting subunit FBXO7 form a functional E3 ubiquitin ligase. FBXO7 is implicated in Parkinson’s disease. In addition to reduced proteasome activity, loss of FBXO7 in mice leads to Parkinsonism-like phenotype. Human FBXO7 is mainly localized to the nucleus, while the mutation observed in patients with parkinsonian-pyramidal syndrome leads to impaired nuclear localization of this protein.Product Details
- Antibody Type
- Host Species
- Human FBXO7 recombinant protein (1-250 a.a.) expressed in E. coli.
- This antibody is provided in 50% glycerol in aqueous buffered solutions with preservatives.
- The antibody was purified by affinity chromatography and conjugated with HRP under optimal conditions.
- 0.5 mg/ml
- Storage & Handling
- Upon receipt, the antibody solution should be stored undiluted at -20°C.
WB - Quality tested
- Recommended Usage
Each lot of this antibody is quality control tested by Western blotting. For Western blotting, the suggested use of this reagent is 2.0 - 5.0 µg per ml. It is recommended that the reagent be titrated for optimal performance for each application.
- Application Notes
This antibody is specific for human FBXO7 and does not cross-react with rat or mouse FBXO7, validated by western blot. The two bands observed in western blot potentially indicate the two isoforms of FBXO7.
AB_2783431 (BioLegend Cat. No. 853503)
AB_2783432 (BioLegend Cat. No. 853504)
- FBXO7 is a 522 amino acid protein with a molecular mass of ~60 kD.
Tissue distribution: FBXO7 is ubiquitously expressed in the many tissues including brain and muscle.
Cellular distribution: Cytoplasmic and nucleus.
- FBXO7 is involved in the ubiquitin-proteasome system, and defects in FBXO7 cause Parkinson's disease-like phenotypes.
- FBXO7 interacts with the members of the SCF (SKP1/cullin‐1/F‐box protein) complex.
- Biology Area
- Cell Biology, Neurodegeneration, Neuroscience, Neuroscience Cell Markers, Protein Trafficking and Clearance
- Molecular Family
- Nuclear Markers
- Antigen References
- Vingill S, et al. 2016. EMBO J. 35: 2008-25.
- Zhao T, et al. 2011. PLoS One. 6:e16983.
- Zhou ZD, et al. 2015. Hum. Mol. Genet. 24:6314-30.
- Gene ID
- 25793 View all products for this Gene ID
- View information about FBXO7 on UniProt.org
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