Gene: SLC1A3
Official Full Name: solute carrier family 1 member 3provided by HGNC
Gene Summary: This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03733 | SLC1A3 Knockout cell line (HeLa) | Human | SLC1A3 | 1:3~1:6 | Negative | Online Inquiry |
KO03734 | SLC1A3 Knockout cell line (HCT 116) | Human | SLC1A3 | 1:2~1:4 | Negative | Online Inquiry |
KO03735 | SLC1A3 Knockout cell line (HEK293) | Human | SLC1A3 | 1:3~1:6 | Negative | Online Inquiry |
SLC1A3 Gene Knockout Cell Lines are genetically engineered cell lines designed to lack the expression of the SLC1A3 gene, which encodes the glutamate transporter EAAT1 (Excitatory Amino Acid Transporter 1). This transporter plays a crucial role in maintaining glutamate homeostasis in the central nervous system, thereby preventing neurotoxicity associated with excessive extracellular glutamate levels. The SLC1A3 gene knockout facilitates the examination of glutamate signaling pathways and their implications in conditions such as epilepsy, neurodegenerative diseases, and psychiatric disorders.
The primary function of these knockout cell lines is to provide a robust platform for functional assays, allowing researchers to investigate the effects of glutamate dysregulation in vitro. By eliminating SLC1A3 expression, these cell lines mimic pathophysiological states, enabling the assessment of cellular responses to glutamate and other neuroactive compounds. This model is invaluable for studying the molecular mechanisms underlying neuronal excitability and synaptic plasticity, crucial for understanding brain function and disease.
The scientific importance of SLC1A3 Gene Knockout Cell Lines is amplified by their applications in both research and clinical settings. They serve as vital tools for drug discovery, particularly in screening novel therapeutics aimed at modulating excitatory neurotransmission. Furthermore, these cell lines provide insight into the functional consequences of gene expression alterations, paving the way for advancements in gene therapy approaches for neurological disorders.
What differentiates these cell lines from alternatives is their targeted genetic modification and the precision of knockout efficiency, ensuring reliable and reproducible results. Enhanced specificity over pharmacological inhibitors, which can have off-target effects, allows for a clearer understanding of glutamate transport and its ramifications in various diseases.
For researchers, clinicians, and pharmaceutical developers, SLC1A3 Gene Knockout Cell Lines represent an essential resource for elucidating complex neurobiological mechanisms and innovating therapeutic strategies. The ability to study the role of SLC1A3 in a controlled environment significantly advances our understanding of neurological health and disease.
Our company specializes in high-quality biological products and cutting-edge genetic engineering techniques, ensuring that our SLC1A3 Gene Knockout Cell Lines meet rigorous scientific standards and provide unparalleled support for your research and clinical applications.
Please note that all services are for research use only. Not intended for any clinical use.
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