Gene: SLC38A1
Official Full Name: solute carrier family 38 member 1provided by HGNC
Gene Summary: Amino acid transporters play essential roles in the uptake of nutrients, production of energy, chemical metabolism, detoxification, and neurotransmitter cycling. SLC38A1 is an important transporter of glutamine, an intermediate in the detoxification of ammonia and the production of urea. Glutamine serves as a precursor for the synaptic transmitter, glutamate (Gu et al., 2001 [PubMed 11325958]).[supplied by OMIM, Mar 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO25770 | SLC38A1 Knockout cell line (HeLa) | Human | SLC38A1 | 1:3~1:6 | Negative | Online Inquiry |
KO25771 | SLC38A1 Knockout cell line (HCT 116) | Human | SLC38A1 | 1:2~1:4 | Negative | Online Inquiry |
KO25772 | SLC38A1 Knockout cell line (HEK293) | Human | SLC38A1 | 1:3~1:6 | Negative | Online Inquiry |
KO25773 | SLC38A1 Knockout cell line (A549) | Human | SLC38A1 | 1:3~1:4 | Negative | Online Inquiry |
SLC38A1 gene knockout cell lines are specialized biological research tools designed to facilitate the study of the solute carrier family 38 member 1 (SLC38A1) gene, which encodes a sodium-dependent neutral amino acid transporter. These knockout cell lines are genetically engineered to disrupt the SLC38A1 gene, providing researchers with a unique model to investigate the physiological and pathological functions of this transporter in various cellular processes, including amino acid transport, metabolic regulation, and contributions to disease states.
The primary mechanism of action for SLC38A1 involves mediating the influx of neutral amino acids into cells, crucial for cellular homeostasis and signaling pathways. By utilizing knockout cell lines, researchers can clearly delineate the effects of SLC38A1 deficiency on cellular metabolism and amino acid balance, offering insights into its role in metabolic disorders and potential therapeutic targets. The loss of this transporter can serve as a valuable model for studying abnormalities in amino acid transport linked to various human diseases, including neurodegenerative disorders and certain types of cancer.
The scientific significance of SLC38A1 gene knockout cell lines extends to their applications in both fundamental research and translational studies. These models enable the exploration of amino acid signaling pathways and their implications in metabolic diseases, while also serving as a screening platform for potential drugs targeting amino acid transporters. Compared to other models, these knockout cell lines provide a more focused approach to studying SLC38A1 without the influence of compensatory mechanisms that might occur in wild-type conditions.
For researchers and clinicians, the availability of SLC38A1 gene knockout cell lines is invaluable. They allow for streamlined investigation of the gene's functional roles, facilitating the discovery and validation of therapeutic interventions aimed at modulating amino acid transport. Additionally, these advanced cell lines come with the assurance of high specificity and reproducibility, which are critical for rigorous scientific inquiry.
Our company is dedicated to providing high-quality biological products and tools that enhance research capabilities. With our extensive expertise in genetic engineering and cell line development, we ensure that our SLC38A1 gene knockout cell lines meet the highest standards of reliability and performance, empowering researchers to achieve their scientific objectives effectively.
Please note that all services are for research use only. Not intended for any clinical use.
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