Gene: DDX11
Official Full Name: DEAD/H-box helicase 11provided by HGNC
Gene Summary: DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an enzyme that possesses both ATPase and DNA helicase activities. This gene is a homolog of the yeast CHL1 gene, and may function to maintain chromosome transmission fidelity and genome stability. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO38255 | DDX11 Knockout cell line (HeLa) | Human | DDX11 | 1:3~1:6 | Negative | Online Inquiry |
KO38256 | DDX11 Knockout cell line (HCT 116) | Human | DDX11 | 1:2~1:4 | Negative | Online Inquiry |
KO38257 | DDX11 Knockout cell line (HEK293) | Human | DDX11 | 1:3~1:6 | Negative | Online Inquiry |
DDX11 Gene Knockout Cell Lines are specifically engineered cellular systems that have undergone targeted gene disruption of the DDX11 gene, which encodes a member of the DEAD-box protein family, implicated in several critical biological processes including RNA metabolism, DNA repair mechanisms, and maintenance of genomic stability. These knockout models are invaluable tools for studying the functional impact of DDX11 depletion on cellular behavior, particularly with respect to its roles in proliferation, apoptosis, and stress responses.
The core mechanism through which DDX11 Gene Knockout Cell Lines operate involves the complete loss of gene expression, allowing researchers to elucidate the downstream effects of DDX11 absence. By employing techniques such as CRISPR-Cas9 mediated gene editing, these cell lines are designed to accurately replicate the physiological conditions of DDX11 dysfunction, enabling advanced investigations into its links to human diseases, including cancer and genetic disorders.
The scientific importance of these knockout models resides in their applications for both fundamental and translational research. In clinical settings, they serve as platforms for drug discovery initiatives and functional genomics studies, where understanding the molecular pathways altered by DDX11 deficiency can lead to targeted therapeutic approaches.
What sets DDX11 Gene Knockout Cell Lines apart from alternative models is their established validation and robustness, ensuring reproducibility and reliability in experimental outcomes. Researchers benefit from the comprehensive characterization of these cell lines, as they offer a unique opportunity to observe the specific phenotypic consequences associated with DDX11 loss of function, facilitating deeper insights into its biological significance.
For researchers and clinicians aiming to advance their understanding of DDX11-related pathways and explore therapeutic strategies, these cell lines represent a critical asset. They deliver precise experimental control over gene function, supporting innovative research endeavors that can translate findings into clinical applications.
Our company prides itself on delivering high-quality biological products that empower scientists in their pursuit of discovery. With a commitment to excellence and a focus on innovation, we ensure that our DDX11 Gene Knockout Cell Lines meet the rigorous standards of the research community.
Please note that all services are for research use only. Not intended for any clinical use.
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