Gene: SLC3A1
Official Full Name: solute carrier family 3 member 1provided by HGNC
Gene Summary: This gene encodes a type II membrane glycoprotein which is one of the components of the renal amino acid transporter which transports neutral and basic amino acids in the renal tubule and intestinal tract. Mutations and deletions in this gene are associated with cystinuria. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35406 | SLC3A1 Knockout cell line (A549) | Human | SLC3A1 | 1:3~1:4 | Negative | Online Inquiry |
SLC3A1 Gene Knockout Cell Lines are genetically engineered cell models specifically designed to disrupt the function of the solute carrier family 3 member 1 (SLC3A1) gene, which encodes a vital protein involved in amino acid transport and cellular nutrient uptake. By employing state-of-the-art CRISPR-Cas9 gene editing technology, these knockout cell lines facilitate the study of SLC3A1’s role in various physiological and pathological processes, including cellular metabolism, nutrient absorption, and pathogenesis of diseases such as cystinuria.
The primary function of SLC3A1 is to act as a transporter, enabling the uptake of cystine and other amino acids across cellular membranes. In our knockout cell lines, the absence of this transporter allows researchers to investigate the cellular and molecular consequences of diminished amino acid transport, thereby providing critical insights into metabolic disorders, drug interactions, and novel therapeutic targets. The unique mechanisms introduced through this knockout approach allow for comprehensive analyses of gene function and cellular responses under various experimental conditions.
The scientific importance of these cell lines lies in their vast applications within research and clinical settings. They serve as valuable models for investigating genetic diseases, drug responsiveness, and the underlying mechanisms of drug resistance, contributing significantly to the fields of pharmacology, toxicology, and metabolic disease research. With increasing emphasis on personalized medicine, these models enable researchers to better understand patient-specific pathways and responses.
Compared to alternative models, our SLC3A1 Gene Knockout Cell Lines offer unmatched specificity and reliability in studying the implications of SLC3A1 gene disruption. Not only do they reduce variability inherent in other experimental systems, such as whole-animal models, but they also enable rapid and reproducible assessments under controlled conditions, enhancing experimental rigor.
For researchers, clinicians, and pharmaceutical companies, the availability of targeted gene knockout cell lines is pivotal for advancing knowledge and developing novel therapies. Their tailored functionality aids in translating basic research findings into clinical applications. Thus, our SLC3A1 Gene Knockout Cell Lines are an indispensable tool for scientists striving to address complex biological questions.
Our commitment to excellence in genetic engineering and our deep understanding of molecular biology underscore our dedication to providing high-quality, reliable products. With cutting-edge technologies and a robust portfolio, we remain at the forefront of advancing biomedical research.
Please note that all services are for research use only. Not intended for any clinical use.
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