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CYLD Knockout Cell Lines

Gene: CYLD

Official Full Name: CYLD lysine 63 deubiquitinaseprovided by HGNC

Gene Summary: This gene is encodes a cytoplasmic protein with three cytoskeletal-associated protein-glycine-conserved (CAP-GLY) domains that functions as a deubiquitinating enzyme. Mutations in this gene have been associated with cylindromatosis, multiple familial trichoepithelioma, and Brooke-Spiegler syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO11090 CYLD Knockout cell line (HeLa) Human CYLD 1:3~1:6 Negative Online Inquiry
KO11091 CYLD Knockout cell line (HCT 116) Human CYLD 1:2~1:4 Negative Online Inquiry
KO11092 CYLD Knockout cell line (HEK293) Human CYLD 1:3~1:6 Negative Online Inquiry
KO11093 CYLD Knockout cell line (A549) Human CYLD 1:3~1:4 Negative Online Inquiry

Background

CYLD Gene Knockout Cell Lines are genetically engineered cellular models specifically designed to lack the CYLD gene, known for its critical role in modulating various signaling pathways, including those involved in inflammation and cancer. By employing a precision genome-editing technique, such as CRISPR/Cas9, these cell lines provide researchers with the ability to study the functional implications of CYLD absence in cellular context, facilitating deeper insights into its biological roles and interactions.

The primary function of CYLD is to act as a deubiquitinating enzyme that regulates the activity of several important signaling proteins involved in key pathways, such as NF-kB and JNK. This mechanism is vital in maintaining cellular homeostasis, influencing processes like apoptosis, immune response, and cell proliferation. Thus, the CYLD Gene Knockout Cell Lines serve as an invaluable tool for elucidating mechanisms of disease, particularly in models of cancer and inflammatory disorders, where aberrant signaling is often a decisive factor.

Scientific research often relies on models that accurately reflect human disease conditions. The CYLD Gene Knockout Cell Lines allow scientists in research and clinical settings to simulate the effects of CYLD disruption, unveiling potential therapeutic targets and identifying biomarkers for disease progression. Their application extends to drug discovery, functional genomics, and mechanistic studies, making them a versatile asset for both academic and pharmaceutical research environments.

A significant advantage of these knockout cell lines is their reproducibility and consistency, allowing for high-throughput screening and comparative studies. Compared to traditional methods of gene silencing, such as RNA interference, these knockout models offer a more complete and permanent loss of gene function, thereby providing clearer insights into gene-specific pathways and cellular behaviors.

For researchers and clinicians aiming to unravel the complexities of cellular signaling in health and disease, CYLD Gene Knockout Cell Lines represent a cutting-edge resource. They empower their users to drive advancements in biomedical research and therapeutic development through high-fidelity, genetically defined tools.

Our company specializes in developing innovative biological products tailored to the evolving needs of the scientific community. With a commitment to quality and reliability, we provide the tools necessary for researchers to pursue impactful discoveries and pioneering therapies.

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

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