Gene: SLC41A2
Official Full Name: solute carrier family 41 member 2provided by HGNC
Gene Summary: Predicted to enable magnesium ion transmembrane transporter activity. Involved in magnesium ion transport. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO25191 | SLC41A2 Knockout cell line (HeLa) | Human | SLC41A2 | 1:3~1:6 | Negative | Online Inquiry |
KO25192 | SLC41A2 Knockout cell line (HCT 116) | Human | SLC41A2 | 1:2~1:4 | Negative | Online Inquiry |
KO25193 | SLC41A2 Knockout cell line (HEK293) | Human | SLC41A2 | 1:3~1:6 | Negative | Online Inquiry |
KO25194 | SLC41A2 Knockout cell line (A549) | Human | SLC41A2 | 1:3~1:4 | Negative | Online Inquiry |
SLC41A2 Gene Knockout Cell Lines are specifically engineered cellular models that have undergone genomic edits to disrupt the SLC41A2 gene, which is implicated in cellular magnesium transport and homeostasis. These knockout cell lines serve as vital tools for researchers exploring the physiological and pathological roles of magnesium in cellular processes. By eliminating the expression of the SLC41A2 gene, these models enable investigations that elucidate the gene's impact on cell viability, signaling pathways, and stress responses.
The principal mechanism of SLC41A2 involves its role as a magnetotransporter, mediating the transport of magnesium ions across the cellular membrane. Disruption of this gene can lead to altered intracellular magnesium concentrations, allowing researchers to observe changes in metabolic functions and cell signaling cascades that may otherwize be masked. This observation is particularly relevant to studies on cardiovascular health, neurobiology, and cancer biology, where magnesium levels have been associated with various disease mechanisms.
The scientific significance of SLC41A2 Gene Knockout Cell Lines extends into both basic research and clinical applications. In research settings, these lines facilitate targeted studies on magnesium's involvement in cellular signaling, providing important insights for drug development and therapeutic interventions. Clinically, understanding the role of SLC41A2 could lead to potential biomarkers for conditions associated with magnesium dysregulation.
In comparison to conventional cell lines or transient transfection approaches, SLC41A2 Gene Knockout Cell Lines offer stable expression profiles and consistent results across experiments. Researchers benefit from the reduced variability and enhanced reproducibility that these lines provide, allowing for more robust data and conclusions.
By focusing on the fundamental mechanisms behind magnesium transport and its implications in health and disease, SLC41A2 Gene Knockout Cell Lines are invaluable to researchers and clinicians alike. Our company specializes in the development of high-quality genetic models and is committed to empowering scientific discovery through innovative biological products that meet the needs of the research community.
Please note that all services are for research use only. Not intended for any clinical use.
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