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SLC52A3 Knockout Cell Lines

Gene: SLC52A3

Official Full Name: solute carrier family 52 member 3provided by HGNC

Gene Summary: This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO30849 SLC52A3 Knockout cell line (HCT 116) Human SLC52A3 1:2~1:4 Negative Online Inquiry
KO30850 SLC52A3 Knockout cell line (A549) Human SLC52A3 1:3~1:4 Negative Online Inquiry

Background

SLC52A3 Gene Knockout Cell Lines are genetically engineered cellular models designed to functionally study the SLC52A3 gene, which encodes a protein crucial for the transport of vitamin B12 (cobalamin) into cells. By creating knockout variants of these cell lines, researchers are afforded a unique opportunity to investigate the biological implications of SLC52A3 deficiency, shedding light on the gene's role in various physiological processes and diseases.

These knockout cell lines operate by utilizing CRISPR/Cas9 technology, which allows for precise editing of the genome. This mechanism effectively disrupts the SLC52A3 gene, leading to a lack of functional protein and thus inhibiting vitamin B12 transport. This interference can elucidate the cellular consequences of impaired vitamin B12 metabolism, thereby enhancing the understanding of its involvement in disorders such as hereditary combined deficiency of vitamin B12 and related metabolism impairments.

The scientific importance of SLC52A3 Gene Knockout Cell Lines is profound. They facilitate groundbreaking research in nutritional biochemistry, molecular genetics, and cell biology, enabling scientists to explore the genetic underpinnings of vitamin B12 transport-related diseases and their potential therapeutic interventions. Clinically, they serve as invaluable tools in drug development processes aimed at treating deficiencies and associated metabolic disorders.

Compared to alternative models, these knockout cell lines offer distinct advantages, including a high degree of specificity and reproducibility in experimental results. While traditional knockout models may involve long timelines and significant resources, the streamlined production of these cell lines allows for quicker turnarounds in research projects.

Researchers and clinicians seeking to advance their work on vitamin B12-related metabolism will find these cell lines invaluable. Their ability to provide insights into disease mechanisms and potential treatments can significantly contribute to breakthroughs in clinical applications and therapeutic strategies.

Our company has extensive expertise in the development of innovative biological products, including advanced gene editing techniques and specialized cell lines that facilitate pioneering research. We pride ourselves on our commitment to supporting scientific discovery with high-quality, reliable products tailored to researchers’ needs.

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

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