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C1orf116 Knockout Cell Lines

Gene: C1orf116

Official Full Name: chromosome 1 open reading frame 116provided by HGNC

Gene Summary: Located in cytosol and plasma membrane. [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
KO19318 C1orf116 Knockout cell line (HeLa) Human C1orf116 1:3~1:6 Negative Online Inquiry
KO19319 C1orf116 Knockout cell line (HCT 116) Human C1orf116 1:2~1:4 Negative Online Inquiry
KO19320 C1orf116 Knockout cell line (A549) Human C1orf116 1:3~1:4 Negative Online Inquiry

Background

C1orf116 Gene Knockout Cell Lines are genetically modified cell lines designed to specifically inhibit the expression of the C1orf116 gene, which is implicated in various biological processes and diseases. By utilizing CRISPR/Cas9 technology, these knockout cell lines provide researchers with essential tools to investigate the function of C1orf116 in cellular pathways, disease mechanisms, and therapeutic responses. The efficient disruption of gene expression facilitates the study of loss-of-function phenotypes, enabling scientists to elucidate the role of C1orf116 in diseases such as cancer and metabolic disorders.

The primary mechanism of action involves the targeted cleavage of the C1orf116 gene, rendering it non-functional. This gene-editing approach allows for precise control over genetic material, a crucial advantage for researchers aiming to explore gene function and regulation systematically. The resultant cell lines exhibit consistent knockout efficiency, providing reliable models for experimental replication and validation.

From a scientific perspective, C1orf116 Gene Knockout Cell Lines are invaluable in research settings, aiding in the discovery of novel biomarkers and therapeutic targets. In clinical applications, these cell lines can assist in the development of personalized medicine strategies by enabling researchers to understand how variations in gene expression correlate with patient-specific disease states.

What sets these cell lines apart from alternatives is their robustness, reproducibility, and the ability to create stable knockout models, which are not only critical for in vitro studies but also pave the way for future in vivo applications. Researchers and clinicians will find these products to be an indispensable addition to their toolkit, facilitating groundbreaking discoveries and advancements in the field.

Our company specializes in providing high-quality biological products tailored to the needs of modern research and clinical applications, ensuring that our customers have access to the most advanced solutions for their scientific inquiries. With our expertise in gene editing technologies, we are committed to supporting our users in achieving their research goals effectively and efficiently.

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

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