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CCNL1 Knockout Cell Lines

Gene: CCNL1

Official Full Name: cyclin L1provided by HGNC

Gene Summary: Predicted to enable cyclin-dependent protein serine/threonine kinase regulator activity. Involved in regulation of RNA splicing. Located in nucleus. Part of cyclin-dependent protein kinase holoenzyme complex. [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
KO18906 CCNL1 Knockout cell line (HeLa) Human CCNL1 1:3~1:6 Negative Online Inquiry
KO18907 CCNL1 Knockout cell line (HCT 116) Human CCNL1 1:2~1:4 Negative Online Inquiry
KO18908 CCNL1 Knockout cell line (HEK293) Human CCNL1 1:3~1:6 Negative Online Inquiry

Background

CCNL1 Gene Knockout Cell Lines are specially designed cellular models where the CCNL1 gene has been inactivated using precise gene editing techniques, such as CRISPR-Cas9. These knockout cell lines are invaluable tools for researchers, enabling the detailed study of the CCNL1 gene's role in various biological processes, including cell cycle regulation, transcriptional control, and developmental biology.

The primary function of the CCNL1 Gene Knockout Cell Lines is to facilitate the exploration of the consequences of CCNL1 gene loss at both the cellular and molecular levels. By comparing these knockout lines to wild-type controls, researchers can elucidate the pathways and mechanisms that CCNL1 influences, shedding light on its potential roles in human diseases, particularly cancer and other proliferative disorders. The absence of CCNL1 can impact critical cellular functions such as mitosis, apoptosis, and gene expression, providing a unique opportunity to delve into the underlying pathophysiology of various conditions.

In research and clinical settings, these cell lines are crucial for drug discovery and targeted therapies where a thorough understanding of gene function is necessary. They serve as platforms for high-throughput screening of therapeutic compounds that might modulate CCNL1-related pathways, thereby identifying novel treatment strategies for diseases associated with aberrations in this gene.

One significant advantage of using CCNL1 Gene Knockout Cell Lines is the precision and efficiency of the gene editing technology used in their development. This specificity greatly reduces off-target effects, ensuring that observed phenotypic changes are attributable to the CCNL1 knockout. Compared to traditional gene silencing techniques, such as RNA interference, these knockout models provide a more robust and permanent solution for studying gene function.

Researchers and clinicians will find these cell lines invaluable for their ability to reproduce in vivo-like conditions, thus accelerating the path from basic research to medical applications. Moreover, our company's expertise in generating high-quality, reliable gene knockout models underlines our commitment to advancing genetic research. By providing meticulously characterized CCNL1 Gene Knockout Cell Lines, we empower the scientific community to unlock new frontiers in gene function and disease understanding.

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

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