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MCOLN3 Knockout Cell Lines

Gene: MCOLN3

Official Full Name: mucolipin TRP cation channel 3provided by HGNC

Gene Summary: This gene encodes one of members of the mucolipin cation channel proteins. Mutation studies of the highly similar protein in mice have shown that the protein is found in cochlea hair cells, and mutant mice show early-onset hearing loss and balance problems. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO08014 MCOLN3 Knockout cell line (HeLa) Human MCOLN3 1:3~1:6 Negative Online Inquiry
KO08015 MCOLN3 Knockout cell line (HCT 116) Human MCOLN3 1:2~1:4 Negative Online Inquiry
KO08016 MCOLN3 Knockout cell line (HEK293) Human MCOLN3 1:3~1:6 Negative Online Inquiry
KO08017 MCOLN3 Knockout cell line (A549) Human MCOLN3 1:3~1:4 Negative Online Inquiry

Background

MCOLN3 Gene Knockout Cell Lines are genetically engineered cellular models designed to specifically lack the expression of the MCOLN3 gene, which encodes a member of the mucolipin family of proteins that play crucial roles in cellular ion transport and lysosomal function. These knockout cell lines provide researchers with invaluable tools for investigating the biological consequences of MCOLN3 deficiency, including its impact on calcium homeostasis, lysosomal integrity, and overall cellular health.

The primary function of the MCOLN3 knockout cells lies in their ability to mimic the molecular pathways associated with various lysosomal storage disorders and other metabolic syndromes. By providing a controlled environment where other variables are minimized, these cell lines allow for detailed studies into the signaling pathways affected by MCOLN3 malfunction. Mechanistically, the absence of this gene facilitates the exploration of how its loss alters intracellular calcium levels and lysosomal pH, thereby influencing processes of autophagy, cell death, and immune responses.

The scientific significance of these knockout cell lines extends to fundamental research in both basic biology and translational medicine, making them invaluable in the quest to elucidate novel therapeutic targets for diseases linked to lysosomal dysfunction, including neurodegenerative disorders. In clinical research setting, these models can be implemented to screen potential drug candidates aimed at restoring normal cellular homeostasis or mitigating the adverse effects of MCOLN3 loss.

With their precise genetic modification, MCOLN3 Gene Knockout Cell Lines offer distinct advantages over standard cell lines, such as more accurate modeling of disease states and enhanced predictability of experimental outcomes. Moreover, unlike alternative models, these cell lines provide a more reliable baseline to evaluate the efficacy of potential therapeutic interventions, thus streamlining the drug development process.

For researchers and clinicians focused on lysosomal biology and related therapeutic avenues, the MCOLN3 Gene Knockout Cell Lines represent a cutting-edge resource that enhances the understanding of cellular mechanisms and paves the way for future innovations in treatment strategies. Our company specializes in producing high-quality, genetically modified cell lines, bringing together extensive scientific expertise and a commitment to supporting groundbreaking research in the biosciences.

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

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