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SLC16A5 Knockout Cell Lines

Gene: SLC16A5

Official Full Name: solute carrier family 16 member 5provided by HGNC

Gene Summary: This gene encodes a member of the monocarboxylate transporter family and the major facilitator superfamily. The encoded protein is localized to the cell membrane and acts as a proton-linked transporter of bumetanide. Transport by the encoded protein is inhibited by four loop diuretics, nateglinide, thiazides, probenecid, and glibenclamide. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO33573 SLC16A5 Knockout cell line (HeLa) Human SLC16A5 1:3~1:6 Negative Online Inquiry
KO33574 SLC16A5 Knockout cell line (HCT 116) Human SLC16A5 1:2~1:4 Negative Online Inquiry
KO33575 SLC16A5 Knockout cell line (A549) Human SLC16A5 1:3~1:4 Negative Online Inquiry

Background

SLC16A5 Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to lack the functional expression of the SLC16A5 gene, which encodes for the monocarboxylate transporter 5 (MCT5). These cell lines serve as a crucial model for studying the metabolic pathways influenced by MCT5, particularly in the context of lactate and pyruvate transport. By eliminating the SLC16A5 gene, researchers can dissect the specific role of MCT5 in cellular respiration and metabolism, providing insights into how alterations in these pathways may impact cellular health and function.

The key function of these knockout cell lines lies in their ability to facilitate studies aimed at understanding the physiological consequences of MCT5 deficiency. In normal cellular environments, MCT5 plays a vital role in modulating pH balance and transporting various monocarboxylates across the plasma membrane, significantly influencing energy metabolism and cellular signaling. By using these knockout lines, researchers can observe the resultant changes in metabolite flux and cellular responses, establishing a clearer understanding of MCT5's contribution to both normal physiology and pathological conditions.

Scientifically, SLC16A5 knockout models are invaluable in both research and clinical settings. They allow for the exploration of metabolic diseases, cancer biology, and neurometabolic disorders, offering potential therapeutic targets. Traditional models may not adequately represent the molecular intricacies involved; thus, these specialized knockout lines deliver precise, reproducible results that accelerate research progress.

A significant advantage of SLC16A5 Gene Knockout Cell Lines is their specificity. Unlike traditional cell lines that express a full complement of genes, these knockout lines create a controlled environment for studying MCT5-related metabolic dysfunctions. This targeted approach reduces the complexity associated with off-target effects and enhances the reliability of experimental outcomes.

For researchers and clinicians focusing on metabolism, using SLC16A5 knockout cell lines promises more accurate models that lead to novel insights and therapeutic strategies. Our company, with a deep-rooted commitment to advancing biological research and providing high-quality genetic tools, ensures that you receive meticulously developed and validated cell lines tailored to your experimental needs. We are dedicated to supporting your breakthroughs in understanding metabolism and related diseases.

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

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