Gene: SLC39A11
Official Full Name: solute carrier family 39 member 11provided by HGNC
Gene Summary: Predicted to enable copper ion transmembrane transporter activity and zinc ion transmembrane transporter activity. Predicted to be involved in zinc ion transmembrane transport. Predicted to be located in Golgi apparatus; nucleus; and plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37497 | SLC39A11 Knockout cell line (HeLa) | Human | SLC39A11 | 1:3~1:6 | Negative | Online Inquiry |
KO37498 | SLC39A11 Knockout cell line (HCT 116) | Human | SLC39A11 | 1:2~1:4 | Negative | Online Inquiry |
KO37499 | SLC39A11 Knockout cell line (HEK293) | Human | SLC39A11 | 1:3~1:6 | Negative | Online Inquiry |
KO37500 | SLC39A11 Knockout cell line (A549) | Human | SLC39A11 | 1:3~1:4 | Negative | Online Inquiry |
SLC39A11 Gene Knockout Cell Lines are genetically modified cell lines specifically engineered to disrupt the SLC39A11 gene, which encodes for a zinc transporter protein involved in cellular zinc homeostasis. These cell lines serve as a powerful tool for researchers aiming to elucidate the physiological roles of zinc in various biological processes, including cell proliferation, apoptosis, and immune response. By utilizing these knockout models, researchers can explore the ramifications of SLC39A11 deficiency on cellular behavior and zinc metabolism, thereby gaining insights into disorders associated with zinc dysregulation.
The primary function of the SLC39A11 gene product is to facilitate the transport of zinc ions across the cellular membrane, a critical mechanism for maintaining intracellular zinc levels. Through the knockout of this gene, these cell lines enable the investigation of altered signaling pathways and metabolic processes attributed to disrupted zinc transport. Such research is invaluable, particularly given zinc's integral role in signaling and enzymatic functions, with repercussions for studies related to cancer, neurodegenerative diseases, and metabolic syndromes.
One of the distinct advantages of using SLC39A11 Gene Knockout Cell Lines lies in their specificity and efficiency compared to other models. Traditional models, such as RNA interference or overexpression systems, may not achieve complete functional ablation of the target gene, introducing variability in experimental outcomes. In contrast, these knockout cell lines offer a reliable approach for consistent experimental results, minimizing off-target effects and providing a clearer understanding of gene function.
For researchers and clinicians, these cell lines represent a valuable resource for advancing knowledge in the field of molecular biology and translational medicine. The ability to study the precise implications of SLC39A11 gene knockout empowers investigators to uncover novel therapeutic targets and therapeutic strategies for diseases linked to zinc dysregulation.
Our company has established a reputation for excellence in providing high-quality biological products, with a commitment to advancing research and clinical applications. By offering SLC39A11 Gene Knockout Cell Lines, we aim to support the scientific community in their quest to unlock the complexities of gene function and contribute to meaningful advancements in health and disease understanding.
Please note that all services are for research use only. Not intended for any clinical use.
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