Gene: FBXL4
Official Full Name: F-box and leucine rich repeat protein 4provided by HGNC
Gene Summary: This gene encodes a member of the F-box protein family, which are characterized by an approximately 40 amino acid motif, the F-box. F-box proteins constitute one subunit of modular E3 ubiquitin ligase complexes, called SCF complexes, which function in phosphorylation-dependent ubiquitination. The F-box domain mediates protein-protein interactions and binds directly to S-phase kinase-associated protein 1. In addition to an F-box domain, the encoded protein contains at least 9 tandem leucine-rich repeats. The ubiquitin ligase complex containing the encoded protein may function in cell-cycle control by regulating levels of lysine-specific demethylase 4A. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO28204 | FBXL4 Knockout cell line (HeLa) | Human | FBXL4 | 1:3~1:6 | Negative | Online Inquiry |
KO28205 | FBXL4 Knockout cell line (HCT 116) | Human | FBXL4 | 1:2~1:4 | Negative | Online Inquiry |
KO28206 | FBXL4 Knockout cell line (HEK293) | Human | FBXL4 | 1:3~1:6 | Negative | Online Inquiry |
KO28207 | FBXL4 Knockout cell line (A549) | Human | FBXL4 | 1:3~1:4 | Negative | Online Inquiry |
FBXL4 Gene Knockout Cell Lines are specialized cellular models engineered to lack the FBXL4 gene, which is pivotal in various biological processes, particularly those involving protein ubiquitination and degradation. This gene is part of the F-box protein family and plays a critical role in the ubiquitin-proteasome system, regulating protein turnover and cellular homeostasis. The knockout of the FBXL4 gene facilitates the study of its role in cellular pathways, metabolic regulation, and potential involvement in disease mechanisms.
These cell lines operate by employing CRISPR/Cas9 technology, allowing for precise gene editing that results in the targeted deletion of the FBXL4 gene. As a consequence, researchers can effectively investigate the physiological and pathological implications of FBXL4 absence in cellular dynamics, including the impact on cellular stress responses, apoptosis, and signaling pathways. The functions lost upon FBXL4 knockout also provide insights into potential pathogenic processes associated with mutations in this gene, enriching our understanding of rare genetic disorders linked to its dysfunction.
The scientific importance of FBXL4 Gene Knockout Cell Lines extends into both research and clinical arenas. They serve as valuable tools for exploring FBXL4-associated cellular mechanisms and elucidating disease pathways, thereby enabling the discovery of novel therapeutic targets. Their utility in validating drug responses or exploring gene therapy techniques makes them essential for advancing translational research.
Compared to alternative models, these knockout cell lines offer higher specificity and reliability in studying the gene’s functions, devoid of compensatory or off-target effects that could confound results. This specificity significantly enhances the robustness of experimental outcomes.
For researchers and clinicians, the FBXL4 Gene Knockout Cell Lines are indispensable for investigating the complexities of gene function and cellular regulation. Our commitment to providing high-quality biological products enables users to conduct innovative research that can lead to breakthroughs in understanding health and disease. With a strong foundation in molecular biology and genetic engineering, our company is poised to support your scientific endeavors with precision and expertise.
Please note that all services are for research use only. Not intended for any clinical use.
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