Gene: SLC2A1
Official Full Name: solute carrier family 2 member 1provided by HGNC
Gene Summary: This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia. [provided by RefSeq, Apr 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00158 | SLC2A1 Knockout cell line (HEK293) | Human | SLC2A1 | 1:3~1:6 | Negative | Online Inquiry |
KO00161 | SLC2A1 Knockout cell line (HeLa) | Human | SLC2A1 | 1:3~1:6 | Negative | Online Inquiry |
KO08272 | SLC2A1 Knockout cell line (HCT 116) | Human | SLC2A1 | 1:2~1:4 | Negative | Online Inquiry |
KO14108 | SLC2A1 Knockout cell line (A549) | Human | SLC2A1 | 1:3~1:4 | Negative | Online Inquiry |
SLC2A1 Gene Knockout Cell Lines are specialized genetic models created to study the function of the SLC2A1 gene, which encodes the glucose transporter-1 (GLUT1). By disrupting this specific gene, researchers can elucidate the pathways and mechanisms associated with glucose metabolism and transport in various cell types. These knockout cell lines serve as invaluable tools for investigating the implications of GLUT1 deficiency, including the associated metabolic disturbances and potential therapeutic targets for conditions such as glucose transporter type 1 deficiency syndrome (GLUT1-DS).
Key functions of the SLC2A1 gene knockout involve altered cellular uptake of glucose, impacting energy production and overall metabolic homeostasis. The loss of GLUT1 activity in these cell lines allows scientists to study compensatory metabolic pathways, assess the impact on cell viability, and investigate the downstream effects on cellular signaling. Consequently, these models are crucial for understanding both basic biological processes and the pathological states linked to altered glucose transport.
Scientifically, SLC2A1 Gene Knockout Cell Lines have significant relevance in research settings focused on metabolic diseases, cancer biology, and neurobiology. They are instrumental for drug screening and development, where the elucidation of GLUT1's role can lead to novel therapeutic approaches for treating diseases linked to glucose dysregulation.
The specific advantages of using SLC2A1 Knockout Cell Lines include the precise genetic modifications, resulting in reproducible and consistent data that is crucial for sound scientific inquiry. Unlike traditional techniques that rely on pharmacological inhibitors, these knockout lines provide a clearer and more direct understanding of the gene's functional role, thereby enhancing the reliability of experimental outcomes.
For researchers, clinicians, and the pharmaceutical industry, the value of the SLC2A1 Gene Knockout Cell Lines is evident; they enable deeper insights into metabolic disorders and foster innovation in therapeutic development. Our company specializes in offering high-quality, validated biological products, and these knockout cell lines exemplify our commitment to providing researchers with the cutting-edge tools necessary for groundbreaking discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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