Gene: CDKL5
Official Full Name: cyclin dependent kinase like 5provided by HGNC
Gene Summary: This gene is a member of Ser/Thr protein kinase family and encodes a phosphorylated protein with protein kinase activity. Mutations in this gene have been associated with X-linked infantile spasm syndrome (ISSX), also known as X-linked West syndrome, and Rett syndrome (RTT). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO07211 | CDKL5 Knockout cell line (HeLa) | Human | CDKL5 | 1:3~1:6 | Negative | Online Inquiry |
KO07212 | CDKL5 Knockout cell line (HCT 116) | Human | CDKL5 | 1:2~1:4 | Negative | Online Inquiry |
KO07213 | CDKL5 Knockout cell line (HEK293) | Human | CDKL5 | 1:3~1:6 | Negative | Online Inquiry |
KO07214 | CDKL5 Knockout cell line (A549) | Human | CDKL5 | 1:3~1:4 | Negative | Online Inquiry |
CDKL5 Gene Knockout Cell Lines are genetically engineered cell models that have been specifically tailored to disrupt the CDKL5 gene function. This gene is critical for proper neuronal development and function, and its mutation is implicated in a range of neurodevelopmental disorders, most notably CDKL5 Deficiency Disorder (CDD). These cell lines allow researchers to study the biological effects of CDKL5 loss and elucidate the pathways involved in neuronal signaling and synaptic function.
The primary mechanism of action of these knockout cell lines relies on the strategic deletion of the CDKL5 gene using techniques such as CRISPR/Cas9 technology. By knocking out this gene, researchers can investigate the downstream effects on cellular pathways, gene expression, and membrane trafficking, providing insights into the etiology and progression of CDD and other associated neurological conditions. This offers a powerful avenue for both basic and translational research, facilitating the identification of potential therapeutic targets.
In terms of scientific significance, CDKL5 Gene Knockout Cell Lines present substantial advantages in neurobiological research, including their ability to mimic disease-specific phenotypes. Researchers can leverage these models for drug discovery, screening potential therapeutic compounds, and exploring gene therapy approaches tailored for CDD.
Compared to alternative models, which may not authentically represent the pathology of CDKL5-related disorders, these knockout cell lines provide a more accurate representation of the human condition, enhancing the reliability of experimental outcomes. This specificity not only increases the validity of research findings but also promotes the development of tailored treatment strategies.
For researchers and clinicians, the availability of CDKL5 Gene Knockout Cell Lines is invaluable. These models enable the translation of scientific discoveries into innovative therapies, ultimately benefiting patients affected by CDKL5-related disorders. Our company prides itself on its expertise in the development of cutting-edge gene-editing technologies and cell line generation, ensuring that our products remain at the forefront of scientific innovation and application in neurology.
Please note that all services are for research use only. Not intended for any clinical use.
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