Gene: SLC22A1
Official Full Name: solute carrier family 22 member 1provided by HGNC
Gene Summary: Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants encoding two different isoforms have been found for this gene, but only the longer variant encodes a functional transporter. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35364 | SLC22A1 Knockout cell line (A549) | Human | SLC22A1 | 1:3~1:4 | Negative | Online Inquiry |
SLC22A1 Gene Knockout Cell Lines are genetically engineered cellular models that lack functional Solute Carrier Family 22 Member 1 (SLC22A1) genes, which are critical for the uptake of various organic cations, including drugs and metabolites. These cell lines provide researchers with a powerful tool to study the physiological and pharmacological roles of SLC22A1, particularly its involvement in drug transport mechanisms and its influence on drug efficacy and toxicity.
The primary function of these knockout cell lines is to serve as a controlled environment to understand how the absence of SLC22A1 affects cellular processes. By employing CRISPR-Cas9 or similar gene-editing technologies, these cell lines exhibit a complete loss of SLC22A1 expression, enabling researchers to investigate the downstream effects on various signaling pathways and metabolic processes. This model is particularly useful in examining how certain therapeutic agents, such as metformin and other antihypertensive drugs, are affected by the lack of this transporter, thereby elucidating the role of SLC22A1 in drug response variability among patients.
The scientific importance of SLC22A1 Gene Knockout Cell Lines extends to their applications in pharmacogenomics, toxicology, and drug discovery. Understanding the transport mechanisms mediated by SLC22A1 can provide insights into drug-drug interactions and adverse drug reactions, paving the way for more personalized treatment strategies. Additionally, these cell lines can facilitate the screening of new compounds, thereby accelerating the drug development process.
Compared to alternative models, such as wild-type cell lines or primary cell cultures, the SLC22A1 Gene Knockout Cell Lines offer better specificity in studying the transporter’s unique functions without the confounding effects of other genes. This specificity significantly enhances the reliability of experimental results, leading to more robust conclusions regarding drug disposition and efficacy.
Investing in SLC22A1 Gene Knockout Cell Lines is crucial for researchers and clinicians who aim to advance their understanding of drug metabolism and optimize therapeutic interventions. With our extensive experience in cellular engineering and genetic modifications, we are committed to providing high-quality biological products that meet the evolving needs of the scientific community. Our expertise ensures researchers can confidently employ these cell lines in their studies to explore novel avenues for enhancing patient care.
Please note that all services are for research use only. Not intended for any clinical use.
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