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Mouse Anti-FBXO7 (AA 357-456) Recombinant Antibody (CBXF-0418) (CBMAB-F0365-CQ)


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Summary

Host Animal
Mouse
Specificity
Human
Clone
CBXF-0418
Antibody Isotype
IgG2a, κ
Application
ELISA, WB

Basic Information

Specificity
Human
Antibody Isotype
IgG2a, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, pH 7.2
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.
Epitope
AA 357-456

Target

Full Name
F-Box Protein 7
Introduction
This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it may play a role in regulation of hematopoiesis. Alternatively spliced transcript variants of this gene have been identified with the full-length natures of only some variants being determined.
Entrez Gene ID
25793
UniProt ID
Q9Y3I1
Alternative Names
F-Box Protein 7; F-Box Only Protein 7; FBX7; PARK15; FBX07; PKPS; FBX;
Research Area
Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Recognizes BIRC2 and DLGAP5. Plays a role downstream of PINK1 in the clearance of damaged mitochondria via selective autophagy (mitophagy) by targeting PRKN to dysfunctional depolarized mitochondria. Promotes MFN1 ubiquitination.
Biological Process
Autophagy of mitochondrion Source: UniProtKB
Negative regulation of cyclin-dependent protein serine/threonine kinase activity Source: Ensembl
Negative regulation of G1/S transition of mitotic cell cycle Source: Ensembl
Negative regulation of hydrogen peroxide-induced neuron death Source: ParkinsonsUK-UCL
Negative regulation of lymphocyte differentiation Source: Ensembl
Negative regulation of oxidative stress-induced neuron death Source: ParkinsonsUK-UCL
Positive regulation of autophagy of mitochondrion Source: ParkinsonsUK-UCL
Protein targeting to mitochondrion Source: UniProtKB
Protein ubiquitination Source: ParkinsonsUK-UCL
Regulation of locomotion Source: ParkinsonsUK-UCL
Regulation of neuron projection development Source: ParkinsonsUK-UCL
Regulation of protein stability Source: UniProtKB
Ubiquitin-dependent protein catabolic process Source: ParkinsonsUK-UCL
Cellular Location
Mitochondrion; Nucleus; Cytoplasm; Cytosol. Predominantly cytoplasmic (PubMed:16096642). A minor proportion is detected in the nucleus (PubMed:16096642). Relocates from the cytosol to depolarized mitochondria (PubMed:23933751).
Involvement in disease
Parkinson disease 15 (PARK15):
A neurodegenerative disorder characterized by parkinsonian and pyramidal signs. Clinical manifestations include tremor, bradykinesia, rigidity, postural instability, spasticity, mainly in the lower limbs, and hyperreflexia.
More Infomation

Zhong, Y., Li, J., Ye, M., & Jin, X. (2022). The characteristics of FBXO7 and its role in human diseases. Gene, 146972.

Palmer, M. C., Neudorf, N. M., Farrell, A. C., Razi, T., Lichtensztejn, Z., & McManus, K. J. (2022). The F-box protein, FBXO7, is required to maintain chromosome stability in humans. Human molecular genetics, 31(9), 1471-1486.

Harris, R., Yang, M., Schmidt, C., Royet, C., Singh, S., Natarajan, A., ... & Laman, H. (2022). Fbxo7 promotes Cdk6 activity to inhibit PFKP and glycolysis in T cells. Journal of Cell Biology, 221(7), e202203095.

Shen, J. Z., Qiu, Z., Wu, Q., Zhang, G., Harris, R., Sun, D., ... & Spruck, C. (2022). A FBXO7/EYA2-SCFFBXW7 axis promotes AXL-mediated maintenance of mesenchymal and immune evasion phenotypes of cancer cells. Molecular Cell, 82(6), 1123-1139.

Noda, S., Sato, S., Fukuda, T., Ueno, S., Tada, N., & Hattori, N. (2022). Impaired mitochondrial accumulation and Lewy pathology in neuron-specific FBXO7-deficient mice. Molecular Brain, 15(1), 1-5.

Lee, S. H., Jung, S., Lee, Y. J., Hyun, M., & Chung, K. C. (2021). FBXO7 triggers caspase 8-mediated proteolysis of the transcription factor FOXO4 and exacerbates neuronal cytotoxicity. Journal of Biological Chemistry, 297(6).

Huang, T., Fang, L., He, R., Weng, H., Chen, X., Ye, Q., & Qu, D. (2021). Fbxo7 and Pink1 play a reciprocal role in regulating their protein levels. Aging (Albany NY), 13(1), 77.

Liu, Y., Lear, T. B., Verma, M., Wang, K. Z., Otero, P. A., McKelvey, A. C., ... & Mallampalli, R. K. (2020). Chemical inhibition of FBXO7 reduces inflammation and confers neuroprotection by stabilizing the mitochondrial kinase PINK1. JCI insight, 5(11).

Correa‐Vela, M., Lupo, V., Montpeyó, M., Sancho, P., Marcé‐Grau, A., Hernández‐Vara, J., ... & Espinós, C. (2020). Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect. Annals of clinical and translational neurology, 7(8), 1436-1442.

Joseph, S., Schulz, J. B., & Stegmüller, J. (2018). Mechanistic contributions of FBXO7 to Parkinson disease. Journal of neurochemistry, 144(2), 118-127.

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For research use only. Not intended for any clinical use.

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