Gene: SLC2A8
Official Full Name: solute carrier family 2 member 8provided by HGNC
Gene Summary: This gene belongs to the solute carrier 2A family, which includes intracellular glucose transporters. Based on sequence comparison, the glucose transporters are grouped into three classes and this gene is a member of class II. The encoded protein, like other members of the family, contains several conserved residues and motifs and 12 transmembrane domains with both amino and carboxyl ends being on the cytosolic side of the membrane. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO02470 | SLC2A8 Knockout cell line (HeLa) | Human | SLC2A8 | 1:3~1:6 | Negative | Online Inquiry |
KO02471 | SLC2A8 Knockout cell line (HCT 116) | Human | SLC2A8 | 1:2~1:4 | Negative | Online Inquiry |
KO02472 | SLC2A8 Knockout cell line (HEK293) | Human | SLC2A8 | 1:3~1:6 | Negative | Online Inquiry |
KO02473 | SLC2A8 Knockout cell line (A549) | Human | SLC2A8 | 1:3~1:4 | Negative | Online Inquiry |
SLC2A8 Gene Knockout Cell Lines are genetically engineered cellular models specifically designed to study the functions and regulatory mechanisms of the solute carrier family 2, facilitated glucose transporter member 8 (SLC2A8) gene. This gene encodes a protein integral to the transport of various substrates, including glucose and myo-inositol, across cell membranes. By knocking out the SLC2A8 gene, researchers can investigate the impact of its absence on cellular metabolism, signaling pathways, and overall cellular function, providing insights essential for understanding various physiological and pathological conditions.
The mechanism underpinning these cell lines involves the targeted disruption of the SLC2A8 gene, achieved through advanced genome-editing techniques like CRISPR-Cas9. This allows for the seamless observation of changes in cellular behavior without the confounding effects that gene overexpression or non-targeted gene alterations may introduce. The SLC2A8 knockouts are particularly relevant in studies related to cancer biology, diabetes, and neurodegenerative diseases, where glucose transport plays a critical role.
The scientific importance of these cell lines extends to their application in drug discovery and disease modeling. They enable researchers to evaluate the efficacy of therapeutics aimed at modulating glucose metabolism and transport, offering the potential to uncover novel therapeutic approaches. The specificity of these models also facilitates straightforward experimental designs, improving reproducibility and validity in findings when compared to heterogeneous or wild-type cell lines.
One of the key advantages of using SLC2A8 Gene Knockout Cell Lines over traditional models is their tailored design for specific research goals, eliminating the background noise that can obscure results in less precise systems. Furthermore, these models are optimized for high-throughput applications, enhancing their usability in large-scale screening processes.
To researchers and clinicians seeking reliable tools for investigating metabolic pathways and disease mechanisms, SLC2A8 Gene Knockout Cell Lines represent a crucial resource. The ability to ensure precise genetic modifications allows for a deeper understanding of glucose transport dynamics and its implications in health and disease. Our company specializes in providing high-quality biological products, backed by years of expertise in genetic engineering and cellular biology, ensuring researchers have access to the innovative solutions they need to advance their work.
Please note that all services are for research use only. Not intended for any clinical use.
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