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SLC19A2 Knockout Cell Lines

Gene: SLC19A2

Official Full Name: solute carrier family 19 member 2provided by HGNC

Gene Summary: This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO31723 SLC19A2 Knockout cell line (HeLa) Human SLC19A2 1:3~1:6 Negative Online Inquiry
KO31724 SLC19A2 Knockout cell line (HCT 116) Human SLC19A2 1:2~1:4 Negative Online Inquiry
KO31725 SLC19A2 Knockout cell line (HEK293) Human SLC19A2 1:3~1:6 Negative Online Inquiry
KO31726 SLC19A2 Knockout cell line (A549) Human SLC19A2 1:3~1:4 Negative Online Inquiry

Background

SLC19A2 Gene Knockout Cell Lines are genetically engineered mammalian cell lines that have undergone targeted disruption of the SLC19A2 gene. This gene encodes the solute carrier family 19 member 2 protein, a critical transporter responsible for the uptake of vitamins and other essential molecules. By eliminating the expression of SLC19A2, these cell lines serve as a powerful tool for studying the biological functions of nutrient transport processes, cellular metabolism, and related disorders, such as folate deficiency, which can lead to significant clinical complications.

The primary function of SLC19A2 Gene Knockout Cell Lines is to facilitate investigations into the role of nutrient transport in health and disease. The knockout mechanism often employs CRISPR-Cas9 technology to achieve precise gene editing, ensuring that researchers can reliably study the resultant phenotypic changes in cellular behavior and response to external nutritional environments. This capability is particularly beneficial in examining pathways related to cancer metabolism, neurological disorders, and embryonic development, where folate and other micronutrients play a fundamental role.

In terms of scientific importance, these knockout cell lines allow researchers to dissect the contributions of SLC19A2 to various health conditions, enabling the development of targeted therapies aimed at restoring normal function. Their applications extend to drug testing, toxicology studies, and basic research investigating gene function, making them indispensable for both academic laboratories and pharmaceutical companies.

Compared to traditional cell lines, SLC19A2 Gene Knockout Cell Lines provide unparalleled specificity and reliability for studying the effects of gene loss in a defined cellular context. Their use can lead to better understanding of nutrient transport mechanisms, which is crucial for developing more effective therapeutic interventions. Moreover, these cell lines present an advantage in high-throughput screening settings, allowing for the rapid assessment of therapeutic candidates that may influence or target nutrient transport pathways.

For researchers and clinicians seeking to advance their understanding of gene function and its implications in health and disease, the SLC19A2 Gene Knockout Cell Lines stand out as a valuable resource. The accessibility of these specialized cell lines enables rapid progress in key research areas, ultimately fostering innovation in treatment strategies. Our company brings to the table extensive expertise in the creation and application of genetically modified cell lines, ensuring that users obtain top-quality, reliable products that meet their unique research needs.

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

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