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FBXL2 Knockout Cell Lines

Gene: FBXL2

Official Full Name: F-box and leucine rich repeat protein 2provided 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 Fbls class and, in addition to an F-box, contains 12 tandem leucine-rich repeats. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO04702 FBXL2 Knockout cell line (HeLa) Human FBXL2 1:3~1:6 Negative Online Inquiry
KO04703 FBXL2 Knockout cell line (HCT 116) Human FBXL2 1:2~1:4 Negative Online Inquiry
KO04704 FBXL2 Knockout cell line (HEK293) Human FBXL2 1:3~1:6 Negative Online Inquiry
KO04705 FBXL2 Knockout cell line (A549) Human FBXL2 1:3~1:4 Negative Online Inquiry

Background

FBXL2 Gene Knockout Cell Lines are meticulously engineered cellular models that exhibit a targeted deletion of the FBXL2 gene, which encodes a protein involved in the ubiquitin-proteasome pathway, a crucial metabolic route for regulating protein turnover and signaling. By knocking out the FBXL2 gene, these cell lines facilitate the unambiguous investigation of its functional role, especially in the context of cellular processes such as cell cycle regulation, apoptosis, and differentiation.

These cell lines operate by employing CRISPR-Cas9 technology, a revolutionary genome-editing tool that allows for highly precise modifications of genomic sequences. The mechanism hinges on the introduction of double-strand breaks at specific loci within the FBXL2 gene, subsequently leading to its knockout via non-homologous end joining. This method imparts a reliable approach to studying the biochemical pathways and molecular interactions that are modulated by FBXL2, providing insight into its implications in pathology, including cancer and metabolic disorders.

The scientific importance of FBXL2 Gene Knockout Cell Lines is underscored by their diverse applications in biomedical research and therapeutic development. Researchers can leverage these models to decipher the gene's contribution to disease mechanisms, serving as a valuable tool in drug discovery and personalized medicine. In clinical settings, the ability to assess the functional consequences of FBXL2 loss enhances our understanding of its role as a potential biomarker or therapeutic target, thereby guiding treatment strategies.

Compared to traditional models, these knockout cell lines boast enhanced specificity and reproducibility in experimental results, minimizing off-target effects commonly associated with older gene-editing techniques. Moreover, the availability of these cell lines aligns perfectly with the rising demand for accurate models that replicate human disease states, making them superior to wild-type or non-specific models.

For researchers, clinicians, and pharmaceutical companies alike, the FBXL2 Gene Knockout Cell Lines represent an invaluable resource for advancing cellular and molecular insights into complex biological systems. Our company is committed to providing high-quality, rigorously validated biological products that empower scientific discovery and innovation in understanding gene function and implications in health and disease.

Please note that all services are for research use only. Not intended for any clinical use.

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