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NLGN2 Knockout Cell Lines

Gene: NLGN2

Official Full Name: neuroligin 2provided by HGNC

Gene Summary: This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO15716 NLGN2 Knockout cell line (HeLa) Human NLGN2 1:3~1:6 Negative Online Inquiry
KO15717 NLGN2 Knockout cell line (HCT 116) Human NLGN2 1:2~1:4 Negative Online Inquiry
KO15718 NLGN2 Knockout cell line (HEK293) Human NLGN2 1:3~1:6 Negative Online Inquiry
KO15719 NLGN2 Knockout cell line (A549) Human NLGN2 1:3~1:4 Negative Online Inquiry

Background

NLGN2 Gene Knockout Cell Lines are specialized cellular models engineered to lack the neuroligin-2 gene (NLGN2), which plays a critical role in synapse formation and neural communication. These cell lines serve as powerful tools for researchers studying the underlying mechanisms of neurodevelopmental disorders and various neurological diseases. By disrupting the NLGN2 gene, these cell lines facilitate the examination of synaptic function, connectivity, and the genetic factors contributing to conditions such as autism spectrum disorders and schizophrenia.

The key function of the NLGN2 Gene Knockout Cell Lines lies in their ability to provide a controlled environment where scientists can observe the direct impact of NLGN2 deficiency on neuronal behavior and synaptic integrity. Through assays and experiments, researchers can analyze changes in synaptic transmission, dendritic development, and the overall excitatory/inhibitory balance in neuronal networks. This mechanistic understanding is vital for the development of targeted therapies and interventions for related neuropsychiatric conditions.

These cell lines hold significant scientific importance for both basic research and clinical applications. They can be used not only to identify potential biomarkers for neurodevelopmental disorders but also to screen for compounds that may restore normal synaptic function. As such, they are indispensable for drug discovery and validation processes, particularly in the arena of personalized medicine.

Compared to alternative models, NLGN2 Gene Knockout Cell Lines offer several unique advantages. They provide a genetic specificity that is difficult to achieve through pharmacological manipulations or traditional animal models, allowing for a more precise analysis of gene function in a controlled laboratory setting. Furthermore, the availability of various cellular formats—such as neuronal-derived lines—enables flexibility for researchers with diverse experimental needs.

For researchers and clinicians focused on understanding complex neurobiological pathways, NLGN2 Gene Knockout Cell Lines represent an invaluable resource. Their applications extend from fundamental biology to therapeutic development, making them a vital component of any researcher's toolkit when investigating synaptic disorders.

Our company prides itself on delivering high-quality biological products that empower scientists across the globe. With a strong commitment to innovation and excellence, we continuously strive to support research that can lead to groundbreaking discoveries and improved clinical outcomes.

Please note that all services are for research use only. Not intended for any clinical use.

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