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MIEF1 Knockout Cell Lines

Gene: MIEF1

Official Full Name: mitochondrial elongation factor 1provided by HGNC

Gene Summary: Enables identical protein binding activity; mitochondrial large ribosomal subunit binding activity; and purine ribonucleotide binding activity. Involved in several processes, including mitochondrial large ribosomal subunit assembly; mitochondrion organization; and regulation of mitochondrion organization. Located in mitochondrial matrix and mitochondrial outer membrane. Implicated in optic atrophy. [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO21718 MIEF1 Knockout cell line (HeLa) Human MIEF1 1:3~1:6 Negative Online Inquiry
KO21719 MIEF1 Knockout cell line (HCT 116) Human MIEF1 1:2~1:4 Negative Online Inquiry
KO21720 MIEF1 Knockout cell line (HEK293) Human MIEF1 1:3~1:6 Negative Online Inquiry
KO21721 MIEF1 Knockout cell line (A549) Human MIEF1 1:3~1:4 Negative Online Inquiry

Background

MIEF1 Gene Knockout Cell Lines are specialized cellular models designed to study the role of the MIEF1 gene, which is critical in regulating mitochondrial dynamics and function. These cell lines are engineered through the CRISPR-Cas9 gene-editing technology to create targeted disruptions in the MIEF1 gene, allowing researchers to investigate its contributions to cellular bioenergetics, apoptosis, and overall cellular metabolism in a controlled environment.

The key functions of MIEF1 involve its integral role in mitochondrial fusion and the maintenance of mitochondrial morphology, crucial for cellular respiration and energy production. By examining MIEF1 knockout cell lines, scientists can elucidate the impact of MIEF1 loss on mitochondrial function, including altered ATP production, increased reactive oxygen species generation, and potential shifts towards a pro-apoptotic state. These insights are vital for understanding diseases where mitochondrial dysfunction plays a role, such as neurodegenerative disorders, metabolic syndromes, and certain cancers.

The scientific importance of MIEF1 Gene Knockout Cell Lines is underscored by their multifaceted applications in research and clinical settings. They facilitate drug discovery by enabling high-throughput screening of compounds targeting mitochondrial pathways, help elucidate disease mechanisms related to mitochondrial dysfunction, and contribute to the development of personalized medicine approaches by providing insights into individual cellular responses to therapies.

Compared to alternative models, such as transient knockdown systems, MIEF1 Gene Knockout Cell Lines offer permanent genetic alterations that provide a more stable and reproducible platform for long-term studies. Additionally, their precise CRISPR-Cas9 modifications eliminate the variability associated with conventional methods, allowing for clearer interpretations of experimental outcomes.

For researchers, clinicians, and pharmaceutical companies, these cell lines present a powerful tool for advancing our understanding of mitochondrial biology and its implications in health and disease. Every experiment on these cell lines supports the broader aim of developing innovative therapeutic strategies to combat mitochondrial-related diseases and enhance patient outcomes. Our company is committed to providing high-quality, reliable biological products, backed by robust scientific expertise and a focus on facilitating cutting-edge research in the field of cellular biology.

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

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