Gene: SLC1A1
Official Full Name: solute carrier family 1 member 1provided by HGNC
Gene Summary: This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect. [provided by RefSeq, Mar 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35411 | SLC1A1 Knockout cell line (HeLa) | Human | SLC1A1 | 1:3~1:6 | Negative | Online Inquiry |
KO35412 | SLC1A1 Knockout cell line (HCT 116) | Human | SLC1A1 | 1:2~1:4 | Negative | Online Inquiry |
KO35413 | SLC1A1 Knockout cell line (HEK293) | Human | SLC1A1 | 1:3~1:6 | Negative | Online Inquiry |
KO35414 | SLC1A1 Knockout cell line (A549) | Human | SLC1A1 | 1:3~1:4 | Negative | Online Inquiry |
SLC1A1 Gene Knockout Cell Lines are specially designed cellular models in which the SLC1A1 gene, responsible for coding the sodium-dependent glutamate transporter, has been inactivated or "knocked out." These cell lines serve as vital tools for researchers aiming to investigate the physiological and pathological roles of SLC1A1 in glutamate homeostasis and neurotransmission. The knockout mechanism typically employs CRISPR-Cas9 technology, ensuring precise gene editing that results in the complete absence of SLC1A1 protein expression.
The key function of SLC1A1 involves the uptake of the neurotransmitter glutamate, a critical component of synaptic signaling in the central nervous system. Neuronal dysfunction due to dysregulation of glutamate levels can lead to conditions such as epilepsy, neurodegenerative diseases, and mood disorders. Employing SLC1A1 knockout cell lines allows researchers to elucidate the implications of altered glutamatergic signaling, understand the cellular consequences of knocked-out functionality, and explore potential therapeutic targets for drug development.
In terms of scientific importance, these cell lines offer significant applications in both research and clinical settings. They facilitate high-throughput screening for compounds that may modulate SLC1A1 activity and can serve as invaluable models for studying associated neurological diseases. Furthermore, variations in glutamate transport dynamics can be assessed, allowing for the evaluation of neuronal resilience and susceptibility to toxic insults.
Compared to alternative models, SLC1A1 knockout cell lines provide a targeted approach that enhances specificity and reproducibility in experimental outcomes. Unlike whole animal models, which can introduce genetic variability and confounding factors, these cell lines offer a streamlined system that allows for controlled manipulations and consistent results.
For researchers and clinicians dedicated to unraveling the complexities of glutamate-related disorders, SLC1A1 gene knockout cell lines present a unique opportunity to unlock new insights that could lead to innovative therapeutic strategies. With a commitment to scientific excellence, our company specializes in advanced gene editing technologies and offers a comprehensive range of knockout cell lines tailored for cutting-edge research, ensuring that our customers have access to high-quality, reliable tools for their studies.
Please note that all services are for research use only. Not intended for any clinical use.
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