Gene: SELENOK
Official Full Name: selenoprotein Kprovided by HGNC
Gene Summary: The protein encoded by this gene belongs to the selenoprotein K family. It is a transmembrane protein that is localized in the endoplasmic reticulum (ER), and is involved in ER-associated degradation (ERAD) of misfolded, glycosylated proteins. It also has a role in the protection of cells from ER stress-induced apoptosis. Knockout studies in mice show the importance of this gene in promoting Ca(2+) flux in immune cells and mounting effective immune response. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec). Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Pseudogenes of this locus have been identified on chromosomes 6 and 19.[provided by RefSeq, Aug 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO14235 | SELENOK Knockout cell line (HeLa) | Human | SELENOK | 1:3~1:6 | Negative | Online Inquiry |
KO14236 | SELENOK Knockout cell line (HCT 116) | Human | SELENOK | 1:2~1:4 | Negative | Online Inquiry |
KO14237 | SELENOK Knockout cell line (HEK293) | Human | SELENOK | 1:3~1:6 | Negative | Online Inquiry |
KO14238 | SELENOK Knockout cell line (A549) | Human | SELENOK | 1:3~1:4 | Negative | Online Inquiry |
SELENOK Gene Knockout Cell Lines represent a breakthrough in cellular and molecular biology, specifically engineered to facilitate the study of the essential selenoprotein, SELENOK (Selenoprotein K). These cell lines have been meticulously designed through targeted gene knockout techniques, allowing researchers to investigate the role of SELENOK in various physiological processes, including antioxidant defense, cellular signaling, and immune response modulation. By eliminating the SELENOK gene, these cell lines provide a controlled environment to assess the downstream effects of selenoprotein deficiency.
The primary mechanism of action lies in the complete abrogation of SELENOK expression, which enables the dissection of its functional roles at the molecular level. This allows for the evaluation of alterations in cellular metabolism, gene expression profiles, and protein interactions that are pivotal for understanding the broader implications of selenoproteins in health and disease. Notably, SELENOK knockout models are instrumental in advancing research surrounding conditions such as cancer, cardiovascular diseases, and neurodegeneration, where selenium homeostasis plays a significant role.
What sets SELENOK Gene Knockout Cell Lines apart from traditional models is their enhanced specificity and reproducibility, facilitated by CRISPR-Cas9 gene editing technology. This precision ensures minimal off-target effects, allowing for more reliable and valid experimental outcomes. Additionally, the availability of these standardized knockout lines enables researchers to streamline their studies, accelerate data collection, and enhance comparability across studies.
For researchers and clinicians focused on cellular behavior or selenoprotein interactions, SELENOK knockout models offer a significant advantage in elucidating the underpinnings of various health conditions. The ability to explore the functions of specific genes in a precise manner can lead to therapeutic discoveries and innovative treatments.
As an organization dedicated to advancing biotechnological solutions, we pride ourselves on our commitment to high-quality product offerings and rigorous scientific standards. Our expertise in gene editing and cell line development ensures that researchers have access to the most reliable and valuable tools for their studies, amplifying the pursuit of scientific knowledge and innovation.
Please note that all services are for research use only. Not intended for any clinical use.
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