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CELF1 Knockout Cell Lines

Gene: CELF1

Official Full Name: CUGBP Elav-like family member 1provided by HGNC

Gene Summary: Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. This gene may play a role in myotonic dystrophy type 1 (DM1) via interactions with the dystrophia myotonica-protein kinase (DMPK) gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03448 CELF1 Knockout cell line (HeLa) Human CELF1 1:3~1:6 Negative Online Inquiry
KO03449 CELF1 Knockout cell line (HCT 116) Human CELF1 1:2~1:4 Negative Online Inquiry
KO03450 CELF1 Knockout cell line (HEK293) Human CELF1 1:3~1:6 Negative Online Inquiry
KO03451 CELF1 Knockout cell line (A549) Human CELF1 1:3~1:4 Negative Online Inquiry

Background

CELF1 Gene Knockout Cell Lines are specialized cellular models engineered to lack the CELF1 gene, which encodes a multifaceted RNA binding protein involved in the regulation of mRNA splicing, stability, and translation. By creating knockout models, researchers can investigate the functional implications of the CELF1 protein in various biological processes and diseases, such as cancer, neurodegeneration, and muscle disorders.

These cell lines operate through a precise genetic editing technique, typically facilitated by CRISPR-Cas9 technology, which enables the targeted alteration of the CELF1 gene. The resulting knockout cells provide a robust platform for studying the loss of CELF1 function, enabling scientists to assess downstream effects on gene expression, protein interactions, and cellular pathways critically influenced by this protein.

The scientific importance of CELF1 Gene Knockout Cell Lines cannot be overstated—the absence of the CELF1 protein sees alterations that provide insight into mechanisms underlying gene regulation and its role in pathophysiology. Particularly in research settings, these models are essential for elucidating the contributions of CELF1 to diseases and potential therapeutic targets, making them invaluable tools for both basic and translational research.

Compared to alternatives such as overexpression systems or wild-type cell lines, the CELF1 Gene Knockout Cell Lines offer distinct advantages, including the ability to study loss-of-function phenotypes without compensatory pathways and more accurately model disease scenarios. Researchers can rely on these models to yield consistent, reproducible data that is pertinent to understanding the complexities of gene regulation in human health.

By incorporating CELF1 Gene Knockout Cell Lines into their research, scientists and clinicians can accelerate their discovery processes, opening doors to novel insights into cellular mechanisms and targeted therapies. Our company, with its extensive expertise in genetic engineering and commitment to providing high-quality biological products, is proud to offer these advanced cell line models to support the research community in advancing scientific knowledge and improving patient outcomes.

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

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