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SLC2A3 Knockout Cell Lines

Gene: SLC2A3

Official Full Name: solute carrier family 2 member 3provided by HGNC

Gene Summary: Enables D-glucose binding activity; dehydroascorbic acid transmembrane transporter activity; and hexose transmembrane transporter activity. Involved in D-glucose import across plasma membrane; galactose transmembrane transport; and transport across blood-brain barrier. Located in aggresome and plasma membrane. Biomarker of Alzheimer's disease; acanthosis nigricans; diabetes mellitus; and type 2 diabetes mellitus. [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO01701 SLC2A3 Knockout cell line (HeLa) Human SLC2A3 1:3~1:6 Negative Online Inquiry
KO01702 SLC2A3 Knockout cell line (HCT 116) Human SLC2A3 1:2~1:4 Negative Online Inquiry
KO01703 SLC2A3 Knockout cell line (HEK293) Human SLC2A3 1:3~1:6 Negative Online Inquiry
KO01704 SLC2A3 Knockout cell line (A549) Human SLC2A3 1:3~1:4 Negative Online Inquiry

Background

SLC2A3 Gene Knockout Cell Lines are specifically engineered cellular models that lack the expression of the SLC2A3 gene, which encodes the glucose transporter type 3 (GLUT3). These cell lines serve as crucial tools for scientists studying glucose metabolism, neuronal function, and various metabolic disorders. By knocking out the SLC2A3 gene, researchers can investigate the direct implications of GLUT3 deficiency on cellular processes, including glucose uptake, energy production, and the overall metabolic profile of the cells.

The primary function of these knockout cell lines revolves around elucidating the role of GLUT3 in glucose homeostasis. By observing the differences in cellular behavior when GLUT3 is absent, researchers can better understand the molecular mechanisms underlying disorders linked to energy metabolism, such as diabetes and neurodegenerative diseases. The specific knockout of the SLC2A3 gene removes a significant regulatory protein from the system, allowing for a clear assessment of how glucose transport influences various metabolic pathways.

The scientific importance of these cell lines extends into diverse applications within both research and clinical settings. They provide a foundation for drug discovery, where potential therapeutic candidates can be tested for efficacy in restoring normal glucose metabolism in GLUT3-deficient models. Furthermore, they are valuable in evaluating the impact of SLC2A3 modifications on disease progression, revealing potential novel biomarkers for early diagnosis and treatment strategies.

One distinct advantage of SLC2A3 Gene Knockout Cell Lines is their ability to create a controlled environment in which the specific contribution of GLUT3 to various diseases can be studied without confounding factors from its functional presence. This targeted approach allows researchers to derive more precise conclusions compared to traditional models where GLUT3 is still expressed.

In a field where efficacy and specificity are paramount, SLC2A3 Gene Knockout Cell Lines stand out as superior alternatives to parental cell lines or non-specific glucose transport inhibitors. Their creation is supported by rigorous validation processes that ensure reliability, enabling researchers and clinicians to pursue innovative solutions with confidence.

As leaders in the development of high-quality, specialized cellular models, our company takes pride in providing researchers with the tools they need to accelerate their findings and contribute to the advancement of scientific knowledge in metabolic health and beyond.

Please note that all services are for research use only. Not intended for any clinical use.

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