Gene: HOMER3
Official Full Name: homer scaffold protein 3provided by HGNC
Gene Summary: This gene encodes a member of the HOMER family of postsynaptic density scaffolding proteins that share a similar domain structure consisting of an N-terminal Enabled/vasodilator-stimulated phosphoprotein homology 1 domain which mediates protein-protein interactions, and a carboxy-terminal coiled-coil domain and two leucine zipper motifs that are involved in self-oligomerization. The encoded protein binds numerous other proteins including group I metabotropic glutamate receptors, inositol 1,4,5-trisphosphate receptors and amyloid precursor proteins and has been implicated in diverse biological functions such as neuronal signaling, T-cell activation and trafficking of amyloid beta peptides. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Mar 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO08203 | HOMER3 Knockout cell line (HeLa) | Human | HOMER3 | 1:3~1:6 | Negative | Online Inquiry |
KO08204 | HOMER3 Knockout cell line (HCT 116) | Human | HOMER3 | 1:2~1:4 | Negative | Online Inquiry |
KO08205 | HOMER3 Knockout cell line (HEK293) | Human | HOMER3 | 1:3~1:6 | Negative | Online Inquiry |
KO08206 | HOMER3 Knockout cell line (A549) | Human | HOMER3 | 1:3~1:4 | Negative | Online Inquiry |
HOMER3 Gene Knockout Cell Lines represent a collection of genetically modified cell lines specifically engineered to have a complete disruption of the HOMER3 gene, which encodes a scaffolding protein involved in synaptic signaling and cellular communication. By employing CRISPR-Cas9 gene editing technology, these cell lines provide an invaluable tool for researchers seeking to elucidate the functional role of HOMER3 in various biological processes and its implications in neurological disorders.
The primary function of the HOMER3 gene revolves around its contribution to the formation and stabilization of glutamate receptors at the synaptic membrane, regulating neurotransmitter signaling pathways. By knocking out the HOMER3 gene, researchers can investigate how its absence affects synaptic plasticity, and related neuronal functions, thereby fostering a better understanding of synaptic dysfunctions involved in conditions such as autism spectrum disorders and schizophrenia.
In scientific and clinical research settings, these knockout cell lines serve as a critical model for dissecting molecular mechanisms underlying psychiatric and neurological disorders. The ability to manipulate the HOMER3 gene also allows elucidation of potential therapeutic targets, facilitating the development of innovative strategies for intervention.
Compared to other alternatives, such as using transient transfection methods, HOMER3 Gene Knockout Cell Lines provide a stable platform for long-term studies, ensuring consistency and reproducibility in experimental results. This stability enhances data reliability and accelerates the pace of discovery.
For researchers and clinicians, the power of HOMER3 Gene Knockout Cell Lines lies in their potential to advance our understanding of complex neurobiological pathways. As a pioneer in the field of gene editing technologies, our company is committed to providing high-quality tools that empower scientists in their quest to unlock the mysteries of gene function and its impact on health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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