Gene: SETDB1
Official Full Name: SET domain bifurcated histone lysine methyltransferase 1provided by HGNC
Gene Summary: This gene encodes a histone methyltransferase which regulates histone methylation, gene silencing, and transcriptional repression. This gene has been identified as a target for treatment in Huntington Disease, given that gene silencing and transcription dysfunction likely play a role in the disease pathogenesis. Alternatively spliced transcript variants of this gene have been described.[provided by RefSeq, Jun 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO02987 | SETDB1 Knockout cell line (HeLa) | Human | SETDB1 | 1:3~1:6 | Negative | Online Inquiry |
KO02988 | SETDB1 Knockout cell line (HCT 116) | Human | SETDB1 | 1:2~1:4 | Negative | Online Inquiry |
KO02989 | SETDB1 Knockout cell line (HEK293) | Human | SETDB1 | 1:3~1:6 | Negative | Online Inquiry |
KO02990 | SETDB1 Knockout cell line (A549) | Human | SETDB1 | 1:3~1:4 | Negative | Online Inquiry |
SETDB1 Gene Knockout Cell Lines are genetically engineered cell models in which the SETDB1 gene has been systematically inactivated. SETDB1 (SET-domain bifurcated 1) encodes a histone methyltransferase that plays a crucial role in gene regulation through histone modification. These knockout cell lines facilitate the study of SETDB1's involvement in epigenetic regulation, cellular differentiation, and oncogenesis by providing a platform to observe the phenotypic and molecular consequences of the gene's absence.
The primary mechanism by which SETDB1 exerts its influence involves methylation of histone H3 at lysine 9 (H3K9me3), an epigenetic modification associated with transcriptional repression. By knocking out SETDB1, researchers can delve into its role in maintaining chromatin architecture and gene expression profiles, thus uncovering the intricate details of cellular processes such as proliferation, apoptosis, and response to external stimuli. These insights are particularly valuable in understanding the pathological mechanisms underlying cancers and other diseases where aberrant gene expression plays a critical role.
The scientific importance of SETDB1 Gene Knockout Cell Lines is underscored by their wide-ranging applications in basic research and clinical settings. They are invaluable for elucidating the pathways modulated by SETDB1 and testing therapeutic strategies aimed at reactivating silenced genes or reversing epigenetic alterations. Compared to alternative cell models, these knockout lines offer a more streamlined approach to study the specific effects of the loss of function of SETDB1, as they eliminate confounding variables that could arise from the presence of functional alleles.
Researchers, clinicians, and pharmaceutical developers will find these cell lines particularly advantageous due to their reliability and consistency in data reproducibility. The availability of these knockout models is a pivotal resource for any laboratory aiming to investigate epigenetic regulation in depth.
Our company specializes in delivering high-quality biological tools for groundbreaking research, and with our SETDB1 Gene Knockout Cell Lines, we provide a powerful instrument for researchers seeking to advance their understanding of epigenetics and discover innovative therapeutic avenues.
Please note that all services are for research use only. Not intended for any clinical use.
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