Home / SLC2A13 Knockout Cell Lines

SLC2A13 Knockout Cell Lines

Gene: SLC2A13

Official Full Name: solute carrier family 2 member 13provided by HGNC

Gene Summary: Enables ATPase binding activity; myo-inositol:proton symporter activity; and protease binding activity. Involved in myo-inositol transport and positive regulation of amyloid-beta formation. Located in cell body; cell projection; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO02431 SLC2A13 Knockout cell line (HeLa) Human SLC2A13 1:3~1:6 Negative Online Inquiry
KO02432 SLC2A13 Knockout cell line (HCT 116) Human SLC2A13 1:2~1:4 Negative Online Inquiry
KO02433 SLC2A13 Knockout cell line (HEK293) Human SLC2A13 1:3~1:6 Negative Online Inquiry
KO02434 SLC2A13 Knockout cell line (A549) Human SLC2A13 1:3~1:4 Negative Online Inquiry

Background

SLC2A13 Gene Knockout Cell Lines are a cutting-edge tool designed for the investigation of glucose transport mechanisms and metabolic processes in various biological contexts. The SLC2A13 gene encodes a member of the facilitative glucose transporter family, which plays a crucial role in the transportation of hexoses across cellular membranes. These cell lines have been engineered to have a complete knockout of the SLC2A13 gene, enabling researchers to study the physiological and pathological consequences of impaired glucose transport and to elucidate the gene's function in cellular metabolism, insulin signaling, and potential links to diseases such as diabetes and cancer.

The primary mechanism by which these knockout cell lines operate involves the absence of SLC2A13, allowing scientists to assess changes in glucose uptake and metabolism compared to wild-type cells. Researchers can utilize these models to explore compensatory mechanisms activated by the lack of this transporter, thereby providing insight into the broader network of glucose homeostasis within the context of cellular stress or disease.

The scientific importance of SLC2A13 Gene Knockout Cell Lines is underscored by their applications in both fundamental research and translational studies. They serve as invaluable platforms for drug discovery, biomarker identification, and investigations into metabolic disorders, making them essential for both academic and pharmaceutical research initiatives.

The unique selling points of these knockout cell lines include their precise genetic modifications, which result in reproducible and consistent results. Unlike alternative models that might involve partial inhibition or transient suppression, our knockout lines provide a definitive framework for understanding the full impact of SLC2A13 loss.

For researchers and clinicians seeking to deepen their understanding of glucose transport and related diseases, SLC2A13 Gene Knockout Cell Lines represent a transformative product. They enable the development of novel therapeutic strategies and have the potential to unveil new metabolic pathways important in human health.

At [Your Company Name], we are committed to advancing biological research through high-quality, innovative products like these knockout cell lines. Our expertise in generating robust genetic models ensures that you will receive tools that meet the rigorous demands of modern science.

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

Get a free quote

If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.

0

There is no product in your cart.