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RNF14 Knockout Cell Lines

Gene: RNF14

Official Full Name: ring finger protein 14provided 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. This protein interacts with androgen receptor (AR) and may function as a coactivator that induces AR target gene expression in prostate. A dominant negative mutant of this gene has been demonstrated to inhibit the AR-mediated growth of prostate cancer. This protein also interacts with class III ubiquitin-conjugating enzymes (E2s) and may act as a ubiquitin-ligase (E3) in the ubiquitination of certain nuclear proteins. Six alternatively spliced transcript variants encoding two distinct isoforms have been reported. [provided by RefSeq, Jan 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO33051 RNF14 Knockout cell line (HeLa) Human RNF14 1:3~1:6 Negative Online Inquiry
KO33052 RNF14 Knockout cell line (HCT 116) Human RNF14 1:2~1:4 Negative Online Inquiry
KO33053 RNF14 Knockout cell line (HEK293) Human RNF14 1:3~1:6 Negative Online Inquiry
KO33054 RNF14 Knockout cell line (A549) Human RNF14 1:3~1:4 Negative Online Inquiry

Background

RNF14 Gene Knockout Cell Lines are specialized cellular models engineered to specifically lack the RNF14 gene, which encodes a RING finger protein that is involved in ubiquitination processes within the cell. This gene knockout technology allows researchers to study the functional consequences of RNF14 depletion and its role in various biological processes, including cell signaling, transcriptional regulation, and cellular stress responses. By utilizing these cell lines, scientists can precisely dissect the pathways influenced by RNF14, thereby gaining insight into the molecular mechanisms underpinning diseases such as cancer, neurodegenerative disorders, and immune dysfunctions.

The core function of RNF14 involves its participation in the ubiquitin-proteasome pathway, a critical regulator of protein degradation, which governs many cellular processes. With the absence of RNF14, these cell lines enable the examination of altered protein dynamics, including changes in the stability of key regulatory proteins. This makes RNF14 Gene Knockout Cell Lines exceptionally valuable for investigations into how disturbances in protein homeostasis may result in pathological conditions.

In terms of scientific importance, these knockout cell lines can serve as powerful tools in both research and clinical laboratories. They are instrumental in drug discovery, allowing for the evaluation of therapeutic compounds targeting pathways modulated by RNF14. Furthermore, they can be used in genomic studies to elucidate the gene’s expression patterns, interactions, and downstream effects, ultimately advancing the understanding of its role in health and disease.

Distinct from alternative models, RNF14 Gene Knockout Cell Lines offer specific advantages, including the ability to create stable, long-term knockouts that facilitate reproducible and reliable experimental outcomes. These cell lines are generated using state-of-the-art CRISPR-Cas9 technology, ensuring a high degree of specificity and efficiency in gene editing, which is critical for robust data generation.

For researchers and clinicians looking to expand the breadth of their investigations into cell biology, these knockout cell lines present a unique opportunity to reveal novel insights into the RNF14 gene's role in various cellular processes. Furthermore, they align perfectly with ongoing efforts to understand the complexities of ubiquitination and its implications in disease mechanisms.

At [Company Name], we are dedicated to providing cutting-edge biological products that empower researchers to achieve their scientific goals. Our expertise in gene editing technologies, combined with a commitment to quality and customer support, makes us a trusted partner in your research endeavors.

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

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