Gene: FBXO11
Official Full Name: F-box protein 11provided by HGNC
Gene Summary: 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 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. It can function as an arginine methyltransferase that symmetrically dimethylates arginine residues, and it acts as an adaptor protein to mediate the neddylation of p53, which leads to the suppression of p53 function. This gene is known to be down-regulated in melanocytes from patients with vitiligo, a skin disorder that results in depigmentation. Polymorphisms in this gene are associated with chronic otitis media with effusion and recurrent otitis media (COME/ROM), a hearing loss disorder, and the knockout of the homologous mouse gene results in the deaf mouse mutant Jeff (Jf), a single gene model of otitis media. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO09759 | FBXO11 Knockout cell line (HeLa) | Human | FBXO11 | 1:3~1:6 | Negative | Online Inquiry |
KO09760 | FBXO11 Knockout cell line (HCT 116) | Human | FBXO11 | 1:2~1:4 | Negative | Online Inquiry |
KO09761 | FBXO11 Knockout cell line (HEK293) | Human | FBXO11 | 1:3~1:6 | Negative | Online Inquiry |
KO09762 | FBXO11 Knockout cell line (A549) | Human | FBXO11 | 1:3~1:4 | Negative | Online Inquiry |
FBXO11 Gene Knockout Cell Lines are genetically engineered cellular models designed to investigate the role of the FBXO11 gene, known for its involvement in various cellular processes including cell cycle regulation and protein degradation pathways. By utilizing CRISPR-Cas9 technology, these knockout cell lines effectively disrupt the expression of the FBXO11 gene, allowing researchers to explore its biological functions and the downstream effects on cellular behavior, signaling cascades, and gene expression.
These cell lines serve several key functions; they provide a powerful tool for dissecting the role of FBXO11 in specific biological contexts, such as apoptosis, cell proliferation, and immune response modulation. The ablation of FBXO11 can lead to observable phenotypic changes that can be quantitatively analyzed, offering insight into its functions and contributions to diseases, including cancer and autoimmune disorders.
In research and clinical settings, the FBXO11 knockout models are instrumental in elucidating the gene's involvement in pathophysiological conditions. They can also be harnessed for the development of potential therapeutic strategies targeting FBXO11-related pathways, making them highly relevant in the fields of pharmacology and genomics.
When compared to traditional methods such as siRNA-mediated knockdown, FBXO11 Gene Knockout Cell Lines provide a more permanent and reliable option for studying gene function. The precise nature of CRISPR-Cas9-mediated knockouts results in a complete ablation of the gene of interest, reducing variable expression levels that often accompany transient knockdown techniques.
For researchers and clinicians aiming to advance their understanding of FBXO11 and its biological implications, these knockout cell lines represent a crucial tool, bridging the gap between genotype and phenotype. Furthermore, they enable the exploration of novel therapeutic avenues, thereby enriching biomedical research.
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Please note that all services are for research use only. Not intended for any clinical use.
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