Gene: EIF3L
Official Full Name: eukaryotic translation initiation factor 3 subunit Lprovided by HGNC
Gene Summary: Enables RNA binding activity. Contributes to translation initiation factor activity. Involved in translational initiation and viral translational termination-reinitiation. Located in membrane. Part of eukaryotic translation initiation factor 3 complex. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO22568 | EIF3L Knockout cell line (HeLa) | Human | EIF3L | 1:3~1:6 | Negative | Online Inquiry |
KO22569 | EIF3L Knockout cell line (HCT 116) | Human | EIF3L | 1:2~1:4 | Negative | Online Inquiry |
KO22570 | EIF3L Knockout cell line (HEK293) | Human | EIF3L | 1:3~1:6 | Negative | Online Inquiry |
KO22571 | EIF3L Knockout cell line (A549) | Human | EIF3L | 1:3~1:4 | Negative | Online Inquiry |
EIF3L Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to lack the eukaryotic initiation factor 3 subunit L (EIF3L). This key component is integral to the translation initiation process in eukaryotic cells, influencing the assembly of the translation initiation complex and thereby modulating protein synthesis. By providing these knockout cell lines, researchers can investigate the role of EIF3L in various biological processes, including gene expression, cellular stress responses, and metabolic regulation, offering critical insights into the molecular mechanics of cellular function and disease states.
The primary function of the EIF3L knockout cell lines is to serve as a vital tool for studying the effects of EIF3L deficiency on ribosome assembly and function. By comparing these knockout lines to their wild-type counterparts, scientists can assess changes in translational efficiency, cell proliferation, and phenotypic alterations that arise from the absence of EIF3L. This is essential for understanding its implications in diseases such as cancer, where deregulated protein synthesis is a hallmark.
The scientific importance of EIF3L Gene Knockout Cell Lines rests in their potential applications within both basic research and clinical settings. In research, they can be used to explore the translational control mechanisms behind various cellular responses (e.g., stress, differentiation), while in clinical applications, these cell lines may facilitate the development of targeted therapies that manipulate the EIF3L pathway to treat diseases characterized by aberrant protein synthesis.
What sets EIF3L Gene Knockout Cell Lines apart from alternative models is their specificity and ability to reflect the natural cellular environment; they are more authentic than generalized knockdowns created through transient transfection. Additionally, these knockout lines maintain stable genetic modifications, allowing for reproducibility and consistency in experimental outcomes.
For researchers and clinicians, the availability of these knockout cell lines can significantly accelerate experimental timelines as they reduce the need for lengthy gene editing processes. Investing in EIF3L Gene Knockout Cell Lines positions your work at the forefront of translational medicine, ultimately paving the way for innovative treatments and therapeutic interventions.
With a commitment to excellence in genetic engineering and molecular biology, our company leverages advanced technologies to provide high-quality products that enhance research capabilities and foster scientific discovery.
Please note that all services are for research use only. Not intended for any clinical use.
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