Home / SLC46A3 Knockout Cell Lines

SLC46A3 Knockout Cell Lines

Gene: SLC46A3

Official Full Name: solute carrier family 46 member 3provided by HGNC

Gene Summary: The protein encoded by this gene is a member of a transmembrane protein family that transports small molecules across membranes. The encoded protein has been found in lysosomal membranes, where it can transport catabolites from the lysosomes to the cytoplasm. This protein has been shown to be an effective transporter of the cytotoxic drug maytansine, which is used in antibody-based targeting of cancer cells. [provided by RefSeq, Dec 2016]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO04682 SLC46A3 Knockout cell line (HeLa) Human SLC46A3 1:3~1:6 Negative Online Inquiry
KO04683 SLC46A3 Knockout cell line (HCT 116) Human SLC46A3 1:2~1:4 Negative Online Inquiry
KO04684 SLC46A3 Knockout cell line (HEK293) Human SLC46A3 1:3~1:6 Negative Online Inquiry
KO04685 SLC46A3 Knockout cell line (A549) Human SLC46A3 1:3~1:4 Negative Online Inquiry

Background

SLC46A3 Gene Knockout Cell Lines are meticulously engineered cellular models that facilitate the study of the SLC46A3 gene, which encodes the proton-coupled folate transporter (PCFT). These knockout cell lines are generated through CRISPR-Cas9 technology, effectively disrupting the SLC46A3 gene to provide a more profound understanding of its role in folate transport and metabolism. By removing the functional gene, researchers can explore the consequences of its absence, allowing for comprehensive studies regarding folate's essential functions in cellular processes, particularly its influence on nucleic acid synthesis, cell proliferation, and overall cellular metabolism.

The SLC46A3 protein is critical for folate absorption in various tissues, particularly in the intestine and brain. By utilizing knockout cell lines, scientists can elucidate mechanisms underlying folate-related disorders, including neural tube defects and certain forms of anemia. These cell lines can also be employed in drug discovery and toxicological studies, assessing how alterations in folate transport affect drug efficacy and cellular responses.

One significant advantage of SLC46A3 Gene Knockout Cell Lines is their specificity in studying the gene's functions without interference from other transporters implicated in folate metabolism. Compared to alternative models, such as whole-organism studies or less targeted genetic manipulation techniques, these knockout cell lines provide a more controlled environment that yields reproducible results, facilitating comparisons across experiments.

Researchers and clinicians benefit from utilizing these cell lines as they offer a powerful tool for investigating therapeutic interventions and understanding the etiology of diseases linked to folate deficiencies. The potential for translational research towards clinical applications is vast, highlighting their utility in developing novel treatment strategies.

Our company prides itself on its commitment to providing high-quality biological tools for the research community. With a strong background in molecular biology and genetic manipulation, we offer innovative products like the SLC46A3 Gene Knockout Cell Lines to enhance scientific inquiry and accelerate the pace of discovery in vital areas of health and disease.

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.