Gene: ATP6V1C2
Official Full Name: ATPase H+ transporting V1 subunit C2provided by HGNC
Gene Summary: This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A,three B, and two G subunits, as well as a C, D, E, F, and H subunit. The V1 domain contains the ATP catalytic site. This gene encodes alternate transcriptional splice variants, encoding different V1 domain C subunit isoforms. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO09247 | ATP6V1C2 Knockout cell line (HeLa) | Human | ATP6V1C2 | 1:3~1:6 | Negative | Online Inquiry |
KO09248 | ATP6V1C2 Knockout cell line (HCT 116) | Human | ATP6V1C2 | 1:2~1:4 | Negative | Online Inquiry |
KO09249 | ATP6V1C2 Knockout cell line (HEK293) | Human | ATP6V1C2 | 1:3~1:6 | Negative | Online Inquiry |
KO09250 | ATP6V1C2 Knockout cell line (A549) | Human | ATP6V1C2 | 1:3~1:4 | Negative | Online Inquiry |
ATP6V1C2 Gene Knockout Cell Lines are engineered cellular models specifically designed for research on the ATP6V1C2 gene, which encodes a subunit of the vacuolar ATPase (V-ATPase) complex. This complex plays a crucial role in proton transport and acidification of intracellular compartments, impacting processes such as cellular homeostasis, membrane dynamics, and signal transduction. By knockout of ATP6V1C2, these cell lines enable direct investigation of the functional consequences of this gene's inactivation, facilitating elucidation of its biological roles and implications in various diseases.
The primary function of these knockout cell lines stems from the disruption of normal V-ATPase activity, allowing researchers to study the physiological effects of impaired acidification. This can lead to insights into specific cell signaling pathways, metabolic alterations, and even contributions to tumor microenvironments where acid-base balance is critical. Furthermore, the use of knockout cell lines provides a valuable tool for high-throughput drug screening and functional genomics studies, where researchers can assess the impact of various treatments on cell viability and behavior in the context of V-ATPase dysfunction.
The scientific importance of ATP6V1C2 Gene Knockout Cell Lines is underscored by their applications in both basic research and clinical settings. They serve as a model to better understand the role of the V-ATPase in cancer biology, neurological disorders, and metabolic diseases, providing vital information that can inspire therapeutic innovations.
One distinct advantage of using these engineered cell lines over traditional models is the specificity and control they offer in experimental design, reducing background variability often encountered in whole-organism studies. This allows for more accurate assessments of gene function and targeted pathway analysis. Additionally, the high reproducibility of results fosters confidence in data generation, making these knockout cell lines indispensable for cutting-edge research.
For researchers and clinicians focused on genetic and molecular mechanisms in health and disease, ATP6V1C2 Gene Knockout Cell Lines represent a powerful and precise investigative tool. They provide a unique opportunity to delve deeper into the contributions of V-ATPase activity in pathological contexts, ultimately driving advancements in diagnostics and therapeutics.
As a company dedicated to delivering innovative research tools, we proudly offer these specialized cell lines, backed by our expertise in genetic engineering and commitment to supporting scientific discovery.
Please note that all services are for research use only. Not intended for any clinical use.
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