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CDKN2C Knockout Cell Lines

Gene: CDKN2C

Official Full Name: cyclin dependent kinase inhibitor 2Cprovided by HGNC

Gene Summary: The protein encoded by this gene is a member of the INK4 family of cyclin-dependent kinase inhibitors. This protein has been shown to interact with CDK4 or CDK6, and prevent the activation of the CDK kinases, thus function as a cell growth regulator that controls cell cycle G1 progression. Ectopic expression of this gene was shown to suppress the growth of human cells in a manner that appears to correlate with the presence of a wild-type RB1 function. Studies in the knockout mice suggested the roles of this gene in regulating spermatogenesis, as well as in suppressing tumorigenesis. Two alternatively spliced transcript variants of this gene, which encode an identical protein, have been reported. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO38604 CDKN2C Knockout cell line (HeLa) Human CDKN2C 1:3~1:6 Negative Online Inquiry
KO38605 CDKN2C Knockout cell line (HCT 116) Human CDKN2C 1:2~1:4 Negative Online Inquiry
KO38606 CDKN2C Knockout cell line (HEK293) Human CDKN2C 1:3~1:6 Negative Online Inquiry
KO38607 CDKN2C Knockout cell line (A549) Human CDKN2C 1:3~1:4 Negative Online Inquiry

Background

CDKN2C Gene Knockout Cell Lines are specially engineered cellular models that have undergone precise modifications to the CDKN2C gene, a critical regulator of the cell cycle. This gene encodes for a protein that functions as a cyclin-dependent kinase inhibitor, thereby playing a pivotal role in controlling cell proliferation and maintaining genomic stability. The knockout of CDKN2C impairs these regulatory functions, enabling researchers to explore the gene's implications in oncogenesis and other pathological conditions associated with uncontrolled cell growth.

The key mechanism of action revolves around the loss of functional CDKN2C protein, which disrupts the normal inhibitory pathways of cyclin-dependent kinase activity. This disruption leads to accelerated cell cycle progression, allowing researchers to study the downstream effects of CDKN2C deficiency, including alterations in apoptosis, senescence, and tumorigenesis. These insights are invaluable for understanding tumor biology, particularly in cancers where CDKN2C loss is implicated, such as glioblastomas and pancreatic cancers.

The scientific importance of CDKN2C Gene Knockout Cell Lines extends to both research and clinical applications. These models serve as essential tools for drug discovery, enabling the identification of potential therapeutic targets and the development of novel anticancer agents. Furthermore, they facilitate the elucidation of molecular pathways involved in cancer progression and resistance mechanisms, providing a significant advantage in the development of personalized medicine strategies.

The unique selling points of our CDKN2C knockouts lie in their precise genetic engineering and ease of use. Compared to alternative models, these cell lines ensure reproducibility and consistency in experimental outcomes, which are critical for robust research findings. They are readily available for screening and can be adapted for various applications, including high-throughput screening and CRISPR-related studies.

For researchers and clinicians alike, these cell lines represent a vital asset in cancer research, offering insights that could drive innovation in therapeutic approaches. The ability to manipulate CDKN2C expression allows for a deeper understanding of cell cycle dynamics, potentially leading to breakthroughs in treatment regimens.

Our company prides itself on delivering high-quality biological products backed by extensive expertise in genetic engineering and cell line development. With a commitment to advancing scientific research and clinical applications, we are dedicated to supporting the scientific community with reliable tools that meet the highest standards of research excellence.

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

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