Gene: PCDH19
Official Full Name: protocadherin 19provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the delta-2 protocadherin subclass of the cadherin superfamily. The encoded protein is thought to be a calcium-dependent cell-adhesion protein that is primarily expressed in the brain. Mutations in this gene on human chromosome X are associated with sporadic infantile epileptic encephalopathy and to a female-restricted form of epilepsy (EFMR; also known as PCDH19RE). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO15312 | PCDH19 Knockout cell line (HEK293) | Human | PCDH19 | 1:3~1:6 | Negative | Online Inquiry |
PCDH19 Gene Knockout Cell Lines are biologically engineered cell lines specifically designed to lack the expression of the PCDH19 gene, which encodes a member of the protocadherin family involved in cell adhesion and signaling. These cell lines are invaluable tools for investigating the pathophysiological roles of PCDH19 in neurodevelopmental disorders, particularly in relation to epilepsy and cognitive impairments associated with PCDH19-related epilepsy, a condition primarily affecting females.
The key function of PCDH19 Gene Knockout Cell Lines lies in their ability to facilitate research on gene function and gene interactions in a controlled environment. By eliminating PCDH19 expression, researchers can assess how its absence affects cellular processes such as neuronal connectivity, synaptogenesis, and susceptibility to excitotoxicity. This mechanistic insight is crucial for understanding the underlying causes of PCDH19-related diseases and for developing targeted therapeutic strategies.
In the realm of scientific research and clinical applications, these cell lines have significant importance. They allow for the systematic study of gene function, drug testing, and the potential development of gene therapies. Moreover, they can be used to create in vitro models that mimic disease states, providing a platform for screening compounds that may mitigate symptoms or reverse pathological processes.
One of the notable advantages of using PCDH19 Gene Knockout Cell Lines over traditional models, such as animal models, is their ability to deliver reproducible and controlled experimental conditions, which can enhance the reliability of the data generated. Additionally, these cell lines are often easier to handle, less costly to maintain, and enable high-throughput screening, which accelerates the pace of research.
For researchers and clinicians investigating the intricacies of neurodevelopmental disorders, PCDH19 Gene Knockout Cell Lines represent an essential resource that can lead to groundbreaking discoveries and improved therapeutic outcomes. Providing a unique opportunity to dissect the molecular and cellular mechanisms involved in PCDH19-related conditions, our company's long-standing expertise in developing elite biological products ensures that users receive high-quality, reliable resources tailored to their research needs.
Please note that all services are for research use only. Not intended for any clinical use.
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