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EIF4E2 Knockout Cell Lines

Gene: EIF4E2

Official Full Name: eukaryotic translation initiation factor 4E family member 2provided by HGNC

Gene Summary: Enables RNA 7-methylguanosine cap binding activity; mRNA cap binding activity; and ubiquitin protein ligase binding activity. Involved in negative regulation of translational initiation; negative regulation of type I interferon-mediated signaling pathway; and rescue of stalled ribosome. Acts upstream of with a positive effect on miRNA-mediated gene silencing by inhibition of translation. Acts upstream of or within negative regulation of translation. Located in P-body. [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO10369 EIF4E2 Knockout cell line (HeLa) Human EIF4E2 1:3~1:6 Negative Online Inquiry
KO10370 EIF4E2 Knockout cell line (HCT 116) Human EIF4E2 1:2~1:4 Negative Online Inquiry
KO10371 EIF4E2 Knockout cell line (HEK293) Human EIF4E2 1:3~1:6 Negative Online Inquiry
KO10372 EIF4E2 Knockout cell line (A549) Human EIF4E2 1:3~1:4 Negative Online Inquiry

Background

EIF4E2 Gene Knockout Cell Lines are specifically engineered cellular models that lack the expression of the EIF4E2 gene, which encodes a critical component in protein translation regulation. By using CRISPR-Cas9 technology, these knockout cell lines allow researchers to study the precise role of EIF4E2 in various biological processes, including oncogenesis, stress response, and cellular signaling pathways.

The key function of EIF4E2 is to bind to eukaryotic initiation factors, facilitating the recruitment of ribosomes to mRNA for translation initiation. In the absence of EIF4E2, researchers can observe alterations in translational control and mRNA stability, ultimately elucidating the gene's impact on cell proliferation, differentiation, and apoptosis. This understanding is crucial since dysregulation of translation is often implicated in diseases such as cancer and neurodegenerative disorders.

From a scientific standpoint, the EIF4E2 Gene Knockout Cell Lines are invaluable in both research and clinical settings. They provide unique insights into the underlying molecular mechanisms at play in diseases where EIF4E2 is overexpressed or mutated. Additionally, these models can be used to screen potential therapeutic targets or compounds that modulate this pathway, bridging the gap between basic research and therapeutic development.

Compared to alternative cell lines that may only dysregulate translation generally or lack the specific genetic background, our EIF4E2 knockout models stand out due to their precision and reliability. They enable high-resolution studies of translational control and allow researchers to generate reproducible and interpretable data critical for advancing scientific knowledge.

For researchers and clinicians looking to deepen their understanding of gene function and inform innovative therapeutic strategies, these knockout cell lines represent a powerful tool. Our company, with years of expertise in cellular engineering and gene editing technologies, is committed to providing cutting-edge products that enhance research capabilities and contribute to scientific advancement.

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

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