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RNF13 Knockout Cell Lines

Gene: RNF13

Official Full Name: ring finger protein 13provided by HGNC

Gene Summary: The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. The specific function of this gene has not yet been determined. Alternatively spliced transcript variants that encode the same protein have been reported. A pseudogene, which is also located on chromosome 3, has been defined for this gene. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO30960 RNF13 Knockout cell line (HeLa) Human RNF13 1:3~1:6 Negative Online Inquiry
KO30961 RNF13 Knockout cell line (HCT 116) Human RNF13 1:2~1:4 Negative Online Inquiry
KO30962 RNF13 Knockout cell line (HEK293) Human RNF13 1:3~1:6 Negative Online Inquiry
KO30963 RNF13 Knockout cell line (A549) Human RNF13 1:3~1:4 Negative Online Inquiry

Background

RNF13 Gene Knockout Cell Lines represent a sophisticated tool for researchers investigating cellular processes influenced by the RNF13 gene, known to play a crucial role in various signaling pathways and cellular functions, including regulation of protein degradation via the ubiquitin-proteasome system. These cell lines are engineered through CRISPR-Cas9 technology to create a complete knockout of the RNF13 gene, enabling researchers to assess the resultant phenotypic changes, explore gene function, and elucidate mechanistic insights into disease states or biological processes.

The key mechanisms underpinning RNF13 Gene Knockout Cell Lines involve the selective inactivation of the RNF13 gene, leading to the loss of RNF13 protein expression. This results in altered cellular behaviors, such as changes in responses to stress, apoptosis, proliferation, and differentiation, crucial for studying a range of diseases, including cancer and neurodegenerative disorders. The ability to systematically evaluate these effects provides significant leverage in experimental design and hypothesis testing.

Scientific importance is underscored through the utility of these cell lines in pioneering research, drug development, and therapeutic interventions. RNF13 suppression has been correlated with various pathophysiological conditions, making these cell lines invaluable for elucidating their roles in disease mechanisms and drug resistance, thus offering insights that are critical in translational research and clinical settings.

What sets RNF13 Gene Knockout Cell Lines apart from alternative models is their stringent validation process, ensuring high specificity and reproducibility. Compared to conventional gene silencing methods, such as RNA interference, CRISPR-Cas9-mediated knockouts provide permanent and precise genome modifications that facilitate long-term studies of gene function without the transient effects associated with other techniques.

For researchers and clinicians, the undeniable value lies in the multifaceted applications these cell lines offer. They empower investigators with the capacity to assess therapeutic targets, explore cellular signaling pathways, and transform fundamental research into tangible clinical insights.

Our company specializes in advanced genetic engineering and cell line development, leveraging state-of-the-art technologies to deliver high-quality biological products that accelerate scientific discovery and innovation. With our RNF13 Gene Knockout Cell Lines, we are committed to supporting the research community’s quest for understanding the complexities of gene function and disease.

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

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