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DCX Knockout Cell Lines

Gene: DCX

Official Full Name: doublecortinprovided by HGNC

Gene Summary: This gene encodes a member of the doublecortin family. The protein encoded by this gene is a cytoplasmic protein and contains two doublecortin domains, which bind microtubules. In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation. The encoded protein appears to direct neuronal migration by regulating the organization and stability of microtubules. In addition, the encoded protein interacts with LIS1, the regulatory gamma subunit of platelet activating factor acetylhydrolase, and this interaction is important to proper microtubule function in the developing cortex. Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex, leading to epilepsy, cognitive disability, subcortical band heterotopia ("double cortex" syndrome) in females and lissencephaly ("smooth brain" syndrome) in males. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]

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Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00070 DCX Knockout cell line (MG-63) Human DCX Negative Online Inquiry

Background

DCX Gene Knockout Cell Lines are specialized cellular models developed for the study of gene function and pathophysiology in neuroscience and developmental biology. By employing advanced CRISPR-Cas9 genome editing technology, these cell lines have undergone precise deletion of the DCX gene, integral to neuronal migration and cortical development. Consequently, researchers can investigate the downstream effects of DCX deficiency, offering insights into neurological disorders such as lissencephaly and schizophrenia.

The primary mechanism of action involves the targeted knockout of the doublecortin (DCX) gene, thereby elucidating its role in cellular processes like microtubule stabilization, which is crucial for neuronal development. This cellular disruption allows scientists to observe and analyze alterations in migration patterns, neurite outgrowth, and synaptic formation, broadening the understanding of how defects at the genetic level can lead to clinically relevant phenotypes.

The scientific importance of DCX Gene Knockout Cell Lines extends into various applications, including drug discovery, gene therapy validation, and identifying potential therapeutic targets. These models provide unmatched experimental systems that mimic human brain developmental pathways, thereby fostering innovation in both academic and clinical research settings.

One distinctive advantage of our DCX Gene Knockout Cell Lines compared to traditional models is their high specificity and efficiency of gene editing, which ensures minimal off-target effects and reliable results. Furthermore, these cell lines come with thorough characterization data, enabling reproducibility and confidence in experimental outcomes.

For researchers and clinicians focused on neurological diseases, utilizing DCX Gene Knockout Cell Lines can drive significant advancements, offering a robust platform for understanding key biological mechanisms and accelerating therapeutic discovery.

As a leader in the development of innovative biological products, our company is dedicated to equipping scientists with high-quality tools to push the boundaries of research and improve clinical practices, ensuring impactful contributions to the field of neuroscience.

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

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