Gene: SHANK3
Official Full Name: SH3 and multiple ankyrin repeat domains 3provided by HGNC
Gene Summary: This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03149 | SHANK3 Knockout cell line (HeLa) | Human | SHANK3 | 1:3~1:6 | Negative | Online Inquiry |
KO03150 | SHANK3 Knockout cell line (HCT 116) | Human | SHANK3 | 1:2~1:4 | Negative | Online Inquiry |
KO03151 | SHANK3 Knockout cell line (HEK293) | Human | SHANK3 | 1:3~1:6 | Negative | Online Inquiry |
KO03152 | SHANK3 Knockout cell line (A549) | Human | SHANK3 | 1:3~1:4 | Negative | Online Inquiry |
SHANK3 Gene Knockout Cell Lines are genetically modified human cell lines designed to investigate the functional role of the SHANK3 gene, which is integral to synaptic structure and function within the central nervous system. These cell lines are produced using advanced CRISPR-Cas9 gene editing technologies, resulting in a specific deletion of the SHANK3 gene, thereby permitting detailed studies on the impact of its absence on cellular behavior, signaling pathways, and synaptic integration.
The key mechanisms of SHANK3 Gene Knockout Cell Lines revolve around their ability to model neurodevelopmental disorders, particularly those associated with autism spectrum disorders and schizophrenia, where alterations in SHANK3 expression have been implicated. These cell lines allow researchers to dissect the pathophysiological mechanisms underlying synaptic dysfunction and neurodevelopmental anomalies. Through in vitro studies, researchers can explore the effects on synaptic plasticity, protein-protein interactions, and neuronal connectivity, leading to insights about potential therapeutic targets.
The scientific importance of these cell lines is underscored by their application in drug discovery and development, enabling high-throughput screening of compounds that might ameliorate synaptic deficits linked to SHANK3 dysfunction. Unlike traditional cellular models, SHANK3 Gene Knockout Cell Lines provide a more accurate representation of human pathology, enhancing translational research efforts.
The advantages of using SHANK3 Gene Knockout Cell Lines extend to their ease of use and reproducibility in experiments. These cell lines can be cultured consistently, providing reliable data sets for experimental replication. Furthermore, they offer unique selling points over alternatives such as human-induced pluripotent stem cells (iPSCs), including reduced variability and quicker turnaround in experimental settings.
For researchers and clinicians focused on neurodevelopmental disorders, SHANK3 Gene Knockout Cell Lines represent a pivotal tool that can advance understanding and treatment exploration. The specificity and robustness of these models present an invaluable resource for disentangling the complexities of synaptic biology.
Our company, with its commitment to delivering cutting-edge biological products, stands at the forefront of genetic research. We provide researchers with the tools necessary to unlock the mysteries of gene function and advance therapeutic innovations in the realm of neurobiology.
Please note that all services are for research use only. Not intended for any clinical use.
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