Gene: MAGI2
Official Full Name: membrane associated guanylate kinase, WW and PDZ domain containing 2provided by HGNC
Gene Summary: The protein encoded by this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral and pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase-like domain, and multiple PDZ domains. It has structural similarity to the membrane-associated guanylate kinase homologue (MAGUK) family. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO10226 | MAGI2 Knockout cell line (HEK293) | Human | MAGI2 | 1:3~1:6 | Negative | Online Inquiry |
MAGI2 Gene Knockout Cell Lines are genetically modified cell lines specifically engineered to lack the expression of the MAGI2 gene, which encodes a multi-PDZ domain protein involved in various cellular processes including cell signaling, adhesion, and synaptic function. By utilizing the CRISPR-Cas9 genome editing technology, these cell lines offer a precise and efficient means to study the biological implications of MAGI2 deficiency in a variety of physiological and pathological contexts.
The primary function of MAGI2 is to act as a scaffolding protein that facilitates protein-protein interactions within the cell, influencing pathways integral to synaptic architecture and neuron-to-neuron communication. The knockout of MAGI2 leads to notable alterations in signal transduction pathways, which researchers can exploit to uncover its role in neurodevelopment and disease processes such as schizophrenia, autism spectrum disorders, and other neurodegenerative conditions.
The scientific importance of MAGI2 Gene Knockout Cell Lines is underscored by their diverse applications in both research and clinical settings. They provide a powerful tool for elucidating gene function, validating drug targets, and screening potential therapeutic agents that may mitigate pathways affected by MAGI2 loss. Researchers can leverage these cell lines to gain insights into molecular mechanisms of disease and contribute to the development of new treatment strategies.
What sets MAGI2 Gene Knockout Cell Lines apart from alternatives is their high specificity and reliability. Unlike other gene-editing methods, the CRISPR-Cas9 system ensures a high rate of successful knockouts, taken together with a lack of off-target effects. Furthermore, these cell lines are rigorously characterized to confirm the absence of MAGI2 protein expression, enabling high-quality experimental outcomes.
For researchers, clinicians, and biopharmaceutical companies, these cell lines represent an invaluable resource for advancing understanding of MAGI2-related pathways and their implications in health and disease. Partnering with us provides access to a well-established platform backed by years of expertise in genomic engineering and cell biology, ensuring that you receive top-quality biological products to support your important work in life sciences.
Please note that all services are for research use only. Not intended for any clinical use.
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