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SLC46A1 Knockout Cell Lines

Gene: SLC46A1

Official Full Name: solute carrier family 46 member 1provided by HGNC

Gene Summary: This gene encodes a transmembrane proton-coupled folate transporter protein that facilitates the movement of folate and antifolate substrates across cell membranes, optimally in acidic pH environments. This protein is also expressed in the brain and choroid plexus where it transports folates into the central nervous system. This protein further functions as a heme transporter in duodenal enterocytes, and potentially in other tissues like liver and kidney. Its localization to the apical membrane or cytoplasm of intestinal cells is modulated by dietary iron levels. Mutations in this gene are associated with autosomal recessive hereditary folate malabsorption disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2013]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO30858 SLC46A1 Knockout cell line (HeLa) Human SLC46A1 1:3~1:6 Negative Online Inquiry
KO30859 SLC46A1 Knockout cell line (HCT 116) Human SLC46A1 1:2~1:4 Negative Online Inquiry
KO30860 SLC46A1 Knockout cell line (HEK293) Human SLC46A1 1:3~1:6 Negative Online Inquiry
KO30861 SLC46A1 Knockout cell line (A549) Human SLC46A1 1:3~1:4 Negative Online Inquiry

Background

SLC46A1 Gene Knockout Cell Lines are specialized cellular models generated through advanced genomic editing techniques to ablate the function of the SLC46A1 gene, which encodes a proton-coupled folate transporter involved in the absorption and transport of folate and related compounds. By creating a targeted knockout of this gene, these cell lines serve as a vital tool for researchers aiming to investigate the physiological roles of folate transport in various cellular contexts.

The primary function of these cell lines lies in their ability to facilitate in-depth studies on folate metabolism, absorption mechanisms, and potential implications in diseases such as cancer and neurological disorders. By utilizing these knockout models, scientists can better understand how the disruption of the SLC46A1 gene affects cellular behavior, including growth, differentiation, and response to drug treatments, thereby identifying potential therapeutic targets.

In terms of scientific importance, SLC46A1 Gene Knockout Cell Lines are invaluable in research settings where folate's role in cellular processes needs to be elucidated. Their applications span drug development, nutritional studies, and the exploration of pathogen-host interactions, providing insights that could lead to groundbreaking advancements in clinical practice.

The unique selling points of these knockout cell lines include their specificity, reproducibility, and the robust genetic background that allows for straightforward phenotypic characterization compared to conventional cell lines or models that may not accurately reflect the absence of gene function. This specificity enhances the reliability of experimental findings and minimizes the confounding variables that are often present in less tailored models.

Researchers and clinicians benefit from using SLC46A1 Gene Knockout Cell Lines as they can yield critical information on the therapeutic potential of targeting folate transport pathways, ultimately guiding novel treatments for conditions linked to impaired folate metabolism. The capacity to manipulate and analyze these gene knockout lines positions them as a premier choice for experimental designs focused on cellular transport mechanisms.

Our company specializes in providing cutting-edge biological products, including genetically modified cell lines that are meticulously validated and characterized, ensuring that researchers have access to reliable tools that enhance the quality of their scientific discoveries. We are committed to supporting the life sciences community with innovative solutions that drive impactful research and clinical advancements.

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

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