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EPM2AIP1 Knockout Cell Lines

Gene: EPM2AIP1

Official Full Name: EPM2A interacting protein 1provided by HGNC

Gene Summary: The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO02703 EPM2AIP1 Knockout cell line (HeLa) Human EPM2AIP1 1:3~1:6 Negative Online Inquiry
KO02704 EPM2AIP1 Knockout cell line (HCT 116) Human EPM2AIP1 1:2~1:4 Negative Online Inquiry
KO02705 EPM2AIP1 Knockout cell line (HEK293) Human EPM2AIP1 1:3~1:6 Negative Online Inquiry

Background

EPM2AIP1 Gene Knockout Cell Lines are specialized cellular models engineered to lack the expression of the EPM2AIP1 gene, which is associated with glycogen metabolism and neurological disorders. These knockout cell lines serve as invaluable tools for elucidating the role of EPM2AIP1 in various biological processes, particularly in understanding its impact on cellular energy homeostasis and neurodegeneration. By creating a targeted disruption of the EPM2AIP1 gene, researchers can investigate the downstream effects on cellular signaling pathways, allowing for a clearer understanding of the gene’s contributions to disease phenotypes.

The primary function of these cell lines is to facilitate research into the molecular mechanisms underlying EPM2AIP1’s involvement in cellular differentiation and survival, particularly in skeletal muscle and neuronal tissues. When the EPM2AIP1 gene is knocked out, cells exhibit altered metabolism and dysregulated signaling pathways, providing insight into the implications of EPM2AIP1 dysfunction. This allows for a deeper investigation into potential therapeutic targets for conditions such as Lafora disease, which is characterized by glycogen accumulation.

Scientifically, the EPM2AIP1 gene knockout cell lines are crucial for both in vitro and in vivo studies aimed at developing interventions for related disorders. Their application extends to drug screening, genetic modeling, and the elucidation of pathogenic mechanisms, thus bridging fundamental research with translational medicine.

In comparison to other knockout models, these EPM2AIP1 cell lines offer distinct advantages by providing a specific focus on the metabolic pathways influenced by this gene, enabling researchers to perform targeted investigations rather than more generalized studies. They are readily adaptable for high-throughput screening, which is essential for accelerating the pace of discovery in a clinical context.

Ultimately, the EPM2AIP1 Gene Knockout Cell Lines represent a critical asset for researchers and clinicians keen to expand their understanding of glycogen metabolism-related conditions. Our company prides itself on delivering high-quality biological products backed by extensive expertise in genetic engineering and cellular model development, ensuring that our customers have access to the best resources for advancing their research and therapeutic aims.

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

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