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PLEKHG2 Knockout Cell Lines

Gene: PLEKHG2

Official Full Name: pleckstrin homology and RhoGEF domain containing G2provided by HGNC

Gene Summary: The protein encoded by this gene is a RhoGTPase that can activate CDC42 by promoting exchange of GDP for GTP on CDC42. The encoded protein is activated by binding to the beta and gamma subunits of heterotrimeric guanine nucleotide-binding protein. Defects in this gene have been associated with leukodystrophy and acquired microcephaly with or without dystonia. [provided by RefSeq, May 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO15055 PLEKHG2 Knockout cell line (HeLa) Human PLEKHG2 1:3~1:6 Negative Online Inquiry
KO15056 PLEKHG2 Knockout cell line (HCT 116) Human PLEKHG2 1:2~1:4 Negative Online Inquiry
KO15057 PLEKHG2 Knockout cell line (HEK293) Human PLEKHG2 1:3~1:6 Negative Online Inquiry
KO15058 PLEKHG2 Knockout cell line (A549) Human PLEKHG2 1:3~1:4 Negative Online Inquiry

Background

PLEKHG2 gene knockout cell lines are engineered cellular models that facilitate the study of the PLEKHG2 gene's role in various biological processes, particularly those related to cell signaling and cytoskeletal dynamics. By utilizing CRISPR-Cas9 technology, these cell lines have been specifically designed to ensure complete disruption of the PLEKHG2 gene, effectively mimicking conditions observed in specific pathophysiological states. The knockout mechanism leads to a loss of function of the gene, allowing researchers to observe the phenotypic consequences of this deletion, which may include alterations in cell morphology, proliferation, and response to external stimuli.

The scientific importance of PLEKHG2 gene knockout cell lines lies in their ability to elucidate the therapeutic targets associated with various diseases, including cancer and neurodegenerative disorders. By providing a robust platform for functional assays, these cell lines can aid in the identification of novel drug targets and the validation of potential therapeutic interventions. Their applications range from fundamental research aimed at understanding basic cellular processes to translational studies that bridge the gap between bench and bedside.

What sets PLEKHG2 gene knockout cell lines apart from traditional wild-type models is the precision of gene editing, ensuring specificity and reproducibility in experimental outcomes. The resulting phenotypes are not only consistent but also provide a more relevant framework for modeling human diseases. Furthermore, these knockout cell lines facilitate high-throughput screening methodologies, significantly accelerating the drug development process.

Researchers and clinicians can greatly benefit from the availability of PLEKHG2 gene knockout cell lines as they represent a pivotal tool for advancing our understanding of gene function and its implications in disease. By leveraging these innovative models, users can enhance the robustness and relevance of their experimental findings.

Our company specializes in providing state-of-the-art biological products, underpinned by rigorous scientific validation and a commitment to supporting cutting-edge research. With extensive expertise in gene editing technologies and cell line development, we are dedicated to equipping researchers with the essential tools needed to unravel complex biological questions.

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

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