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MCPH1 Knockout Cell Lines

Gene: MCPH1

Official Full Name: microcephalin 1provided by HGNC

Gene Summary: This gene encodes a DNA damage response protein. The encoded protein may play a role in G2/M checkpoint arrest via maintenance of inhibitory phosphorylation of cyclin-dependent kinase 1. Mutations in this gene have been associated with primary autosomal recessive microcephaly 1 and premature chromosome condensation syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO07264 MCPH1 Knockout cell line (HeLa) Human MCPH1 1:3~1:6 Negative Online Inquiry
KO07265 MCPH1 Knockout cell line (HCT 116) Human MCPH1 1:2~1:4 Negative Online Inquiry
KO07266 MCPH1 Knockout cell line (HEK293) Human MCPH1 1:3~1:6 Negative Online Inquiry
KO07267 MCPH1 Knockout cell line (A549) Human MCPH1 1:3~1:4 Negative Online Inquiry

Background

MCPH1 Gene Knockout Cell Lines are a sophisticated biological research tool designed to facilitate the study of microcephaly and related neurodevelopmental disorders. These cell lines have been genetically engineered to disable the MCPH1 gene, which is critically involved in brain development. The knockout of this gene allows researchers to investigate its specific roles in cellular processes such as cell division, DNA repair, and neuronal differentiation, which can be pivotal in understanding the molecular mechanisms underlying human brain size and function.

The key functions of the MCPH1 Gene Knockout Cell Lines include the alteration of cellular signaling pathways that impact neurogenesis, as well as enhanced sensitivity to agents that cause stress or impair cell cycle progression. By utilizing these cell lines, researchers can elucidate the dysregulation of fundamental cellular mechanisms that lead to microcephaly, thus offering insights into potential therapeutic targets for intervention in neurodevelopmental diseases.

The scientific importance of these cell lines extends to both academic and clinical applications. In research settings, they serve as invaluable models for studying the genetic basis of microcephaly, while in clinical contexts, they could facilitate the development of gene therapies or other medical interventions targeted at patients with neurodevelopmental disorders.

Unique selling points of MCPH1 Gene Knockout Cell Lines include their specificity and versatility; they provide a focused approach to studying microcephaly without the confounding effects of other genetic variations. Additionally, these cell lines are available in various formats, including immortalized and primary cell types, making them suitable for diverse experimental designs.

Ultimately, the value of MCPH1 Gene Knockout Cell Lines lies in their ability to empower researchers and clinicians with the means to uncover the intricacies of brain development at a molecular level. This product aligns with our company’s commitment to advancing scientific understanding through high-quality, innovative biological solutions that address pressing health challenges. With expertise in genetic engineering and a portfolio of cutting-edge research tools, we are dedicated to supporting the scientific community in their quest for knowledge and therapeutic advancements.

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

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