Gene: DCAF17
Official Full Name: DDB1 and CUL4 associated factor 17provided by HGNC
Gene Summary: This gene encodes a nuclear transmembrane protein that associates with cullin 4A/damaged DNA binding protein 1 ubiquitin ligase complex. Mutations in this gene are associated with Woodhouse-Sakati syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO26250 | DCAF17 Knockout cell line (HeLa) | Human | DCAF17 | 1:3~1:6 | Negative | Online Inquiry |
KO26251 | DCAF17 Knockout cell line (HCT 116) | Human | DCAF17 | 1:2~1:4 | Negative | Online Inquiry |
KO26252 | DCAF17 Knockout cell line (HEK293) | Human | DCAF17 | 1:3~1:6 | Negative | Online Inquiry |
KO26253 | DCAF17 Knockout cell line (A549) | Human | DCAF17 | 1:3~1:4 | Negative | Online Inquiry |
DCAF17 Gene Knockout Cell Lines are genetically modified cell lines that have had the DCAF17 gene specifically inactivated through homology-directed repair. This product provides invaluable resources for researchers investigating the role of DCAF17 in cellular processes, particularly in relation to protein homeostasis, ubiquitination, and signal transduction. By knocking out the DCAF17 gene, these cell lines offer insights into various biological pathways influenced by this key regulator, allowing for a deeper understanding of disease mechanisms.
The primary function of DCAF17 Gene Knockout Cell Lines lies in their ability to elucidate the cellular consequences of DCAF17 absence. In normal physiology, DCAF17 serves as a substrate receptor for the Cullin-RING E3 ubiquitin ligase complex, which directs protein degradation. Disruption of this pathway can reveal critical regulatory mechanisms affecting cell cycle progression, apoptosis, and cellular stress response, making the knockout cell lines an essential tool for studying cancers and other pathologies linked to protein misfolding or degradation.
The scientific importance of these cell lines extends to both research and clinical settings, where they can be used to screen for novel therapeutic compounds that restore or compensate for the functions lost due to DCAF17 knockout. Additionally, they serve as models for investigating the potential impacts of DCAF17 in drug resistance and therapeutic efficacy, particularly in oncology.
Compared to other gene knockout models, DCAF17 Gene Knockout Cell Lines provide unique advantages, including specificity in DCAF17 disruption and the delivery of reproducible results across different experiments. Their established use in various research environments enhances reliability and accelerates the pace of discovery, making them a preferred choice for investigators.
Researchers and clinicians looking for tools to dissect the molecular intricacies of DCAF17-related pathways will find significant value in these cell lines. By facilitating the identification of potential drug targets and biomarkers, they contribute to advancements in personalized medicine and targeted therapies.
Our company specializes in cutting-edge biotechnological solutions and has developed these DCAF17 Gene Knockout Cell Lines with precision and care, ensuring that they meet the highest standards of quality and efficacy for researchers aiming to expand their understanding of gene function and regulation in health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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