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COX14 Knockout Cell Lines

Gene: COX14

Official Full Name: cytochrome c oxidase assembly factor COX14provided by HGNC

Gene Summary: This gene encodes a small single-pass transmembrane protein that localizes to mitochondria. This protein may play a role in coordinating the early steps of cytochrome c oxidase (COX; also known as complex IV) subunit assembly and, in particular, the synthesis and assembly of the COX I subunit of the holoenzyme. Mutations in this gene have been associated with mitochondrial complex IV deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO24368 COX14 Knockout cell line (HeLa) Human COX14 1:3~1:6 Negative Online Inquiry
KO24369 COX14 Knockout cell line (HCT 116) Human COX14 1:2~1:4 Negative Online Inquiry
KO24370 COX14 Knockout cell line (HEK293) Human COX14 1:3~1:6 Negative Online Inquiry
KO24371 COX14 Knockout cell line (A549) Human COX14 1:3~1:4 Negative Online Inquiry

Background

COX14 Gene Knockout Cell Lines are genetically engineered cell lines in which the COX14 gene, which encodes a protein implicated in cytochrome c oxidase (CcO) assembly and function, has been selectively disrupted. This knockout model serves as an invaluable tool for researchers interested in elucidating the role of COX14 in mitochondrial physiology and pathophysiology. By generating a specific genetic alteration, these cell lines allow for the study of impaired mitochondrial function, providing insights into conditions such as neurodegenerative diseases where mitochondrial dysfunction is often a central theme.

The primary function of the COX14 gene product is to facilitate the proper assembly of the CcO complex, a critical component of the electron transport chain that drives ATP production via oxidative phosphorylation. The disruption of COX14 can result in a diminished CcO activity, which translates into impaired cellular respiration and energy metabolism. This mechanistic understanding is crucial in research fields ranging from metabolic disorders to aging, and even in cancer biology, where altered mitochondrial dynamics play a significant role.

The scientific importance of COX14 Gene Knockout Cell Lines lies in their extensive applicability within both basic and translational research settings. They serve as a model for studying mitochondrial dysfunction mechanisms and evaluating potential therapeutic approaches targeting energy metabolism. Researchers can use these cell lines to assess the impact of novel compounds on mitochondrial health or to explore the genetic interactions affecting oxidative metabolism.

Compared to traditional cell lines or models that do not exhibit specific mitochondrial defects, COX14 knockout cell lines offer unique advantages, including a clear and reproducible phenotype that can be used to dissect mitochondrial pathways with precision. Furthermore, these cell lines can be integrated with various high-throughput screening processes for drug discovery, enabling rapid identification of compounds that can restore normal mitochondrial function.

For researchers and clinicians dedicated to understanding mitochondrial diseases or exploring therapeutic options for disorders resulting from oxidative stress, COX14 Gene Knockout Cell Lines present an essential resource. They embody a sophisticated approach to dissecting complex biological processes and contribute to advancing our understanding of human health and disease.

Our company specializes in providing high-quality biological products, including genetically modified models that empower researchers to make significant strides in their scientific endeavors. With a commitment to excellence and innovation in biotechnology, we deliver tools that enhance research capabilities and promote breakthroughs in health sciences.

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

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