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ATP6V0E2 Knockout Cell Lines

Gene: ATP6V0E2

Official Full Name: ATPase H+ transporting V0 subunit e2provided by HGNC

Gene Summary: Multisubunit vacuolar-type proton pumps, or H(+)-ATPases, acidify various intracellular compartments, such as vacuoles, clathrin-coated and synaptic vesicles, endosomes, lysosomes, and chromaffin granules. H(+)-ATPases are also found in plasma membranes of specialized cells, where they play roles in urinary acidification, bone resorption, and sperm maturation. Multiple subunits form H(+)-ATPases, with proteins of the V1 class hydrolyzing ATP for energy to transport H+, and proteins of the V0 class forming an integral membrane domain through which H+ is transported. ATP6V0E2 encodes an isoform of the H(+)-ATPase V0 e subunit, an essential proton pump component (Blake-Palmer et al., 2007 [PubMed 17350184]).[supplied by OMIM, Mar 2008]

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Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO19574 ATP6V0E2 Knockout cell line (HeLa) Human ATP6V0E2 1:3~1:6 Negative Online Inquiry
KO19575 ATP6V0E2 Knockout cell line (HCT 116) Human ATP6V0E2 1:2~1:4 Negative Online Inquiry
KO19576 ATP6V0E2 Knockout cell line (HEK293) Human ATP6V0E2 1:3~1:6 Negative Online Inquiry
KO19577 ATP6V0E2 Knockout cell line (A549) Human ATP6V0E2 1:3~1:4 Negative Online Inquiry

Background

ATP6V0E2 Gene Knockout Cell Lines are precision-engineered cellular models designed for the functional study of the ATP6V0E2 gene, which encodes a vital component of the vacuolar ATPase complex involved in cellular pH regulation and vesicular trafficking. By employing targeted genome-editing techniques such as CRISPR/Cas9, these cell lines have been generated to eliminate the expression of ATP6V0E2, allowing researchers to investigate its biological roles and implications in various health conditions.

The primary function of ATP6V0E2 is to contribute to proton transport across endosomal and lysosomal membranes, thus influencing autophagy, apoptosis, and intracellular degradation pathways. The knockout of this gene enables researchers to elucidate its specific roles in cellular metabolism and signaling pathways, providing insights into the mechanistic underpinnings of diseases such as cancer and neurodegenerative disorders, where altered lysosomal function is frequently observed.

The scientific importance of ATP6V0E2 knockout cell lines extends into both basic research and clinical applications. These cell lines are invaluable for advancing drug discovery initiatives by serving as models for testing potential therapeutic agents that target vacuolar ATPase activity. Additionally, they facilitate disease modeling, allowing for the assessment of gene function and the impact of ATP6V0E2 deficiency on cellular phenotypes.

Compared to alternative cell lines, ATP6V0E2 knockout models offer superior specificity and reliability, ensuring that experimental outcomes are not confounded by the presence of residual gene function. This specificity enhances the reproducibility of research findings and improves the translational potential of studies aiming to develop ATP6V0E2-targeted therapies.

For researchers and clinicians in the fields of molecular biology, pharmacology, and genetics, these knockout cell lines provide a powerful toolset for exploration and innovation. The ability to manipulate and study the consequences of ATP6V0E2 loss-of-function positions these cell lines as essential resources for a deeper understanding of cell biology and disease mechanisms.

Our company prides itself on cutting-edge genetic engineering technologies and a commitment to enhancing research capabilities. Through our expertise, we deliver high-quality, biologically relevant models that empower scientists to accelerate their discoveries and contribute to advancements in health and medicine.

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

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