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SLC17A9 Knockout Cell Lines

Gene: SLC17A9

Official Full Name: solute carrier family 17 member 9provided by HGNC

Gene Summary: This gene encodes a member of a family of transmembrane proteins that are involved in the transport of small molecules. The encoded protein participates in the vesicular uptake, storage, and secretion of adenoside triphosphate (ATP) and other nucleotides. A mutation in this gene was found in individuals with autosomal dominant disseminated superficial actinic porokeratosis-8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00355 SLC17A9 Knockout cell line (HeLa) Human SLC17A9 1:3~1:6 Negative Online Inquiry
KO20132 SLC17A9 Knockout cell line (HCT 116) Human SLC17A9 1:2~1:4 Negative Online Inquiry

Background

SLC17A9 Gene Knockout Cell Lines are specifically engineered cellular models that lack the SLC17A9 gene, which encodes a protein involved in the transport of certain neurotransmitters, notably ATP. These knockout cell lines serve as a vital resource for understanding the physiological roles of SLC17A9 within various biological contexts, including neuronal signaling and cellular metabolism. By employing CRISPR-Cas9 gene editing techniques, these cells demonstrate a precise alteration of the genome, allowing researchers to study the consequent metabolic and phenotypic changes that arise from the absence of this gene.

The primary function of the SLC17A9 gene is to facilitate the vesicular transport of ATP, contributing to neurotransmitter release in the synaptic cleft. Without its expression, researchers can elucidate the impacts on signaling pathways, cellular homeostasis, and potential biochemical cascades that are triggered by ATP's absence in both in vitro and in vivo experiments. This model is particularly significant in neuroscience and cellular biology research, where understanding ATP's role in signaling and energy metabolism can lead to new therapeutic strategies for neurological disorders.

One of the unique advantages of the SLC17A9 Gene Knockout Cell Lines is their specificity and precision in targeting the gene of interest, compared to other methods such as RNA interference, which may lead to off-target effects and incomplete gene repression. This specificity allows for clearer interpretation of results, making it a superior choice for rigorous scientific inquiry. Furthermore, these knockout cell lines can be utilized in drug discovery and development with enhanced confidence, given their ability to provide insights into the mechanisms of action and potential side effects of pharmaceutical compounds.

Researchers and clinicians will find the SLC17A9 Gene Knockout Cell Lines valuable tools in advancing their understanding of cellular transport mechanisms and their implications for disease models. As a leading provider of innovative biological research products, our company prides itself on delivering high-quality tools that enhance scientific progress. Our expertise ensures that we meet the evolving needs of researchers in their quest for discoveries that can transform therapeutic approaches.

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

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