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TIMM17A Knockout Cell Lines

Gene: TIMM17A

Official Full Name: translocase of inner mitochondrial membrane 17Aprovided by HGNC

Gene Summary: Predicted to contribute to protein transmembrane transporter activity. Predicted to be involved in protein import into mitochondrial matrix. Located in mitochondrial inner membrane and nucleoplasm. Part of TIM23 mitochondrial import inner membrane translocase complex. [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
KO31864 TIMM17A Knockout cell line (HeLa) Human TIMM17A 1:3~1:6 Negative Online Inquiry
KO31865 TIMM17A Knockout cell line (HCT 116) Human TIMM17A 1:2~1:4 Negative Online Inquiry
KO31866 TIMM17A Knockout cell line (HEK293) Human TIMM17A 1:3~1:6 Negative Online Inquiry
KO31867 TIMM17A Knockout cell line (A549) Human TIMM17A 1:3~1:4 Negative Online Inquiry

Background

TIMM17A Gene Knockout Cell Lines are engineered cellular models that lack the expression of the TIMM17A gene, which encodes for a vital component of the mitochondrial translocase of the inner membrane. This gene plays a crucial role in mitochondrial protein import and, by extension, mitochondrial biogenesis. The knockout of TIMM17A allows researchers to investigate the repercussions of impaired mitochondrial import processes and the resultant metabolic dysfunctions, making these cell lines essential tools for studying mitochondrial biology and related disorders.

The key functions of TIMM17A Gene Knockout Cell Lines include their ability to model mitochondrial dysfunction. By removing this gene, these cell lines can elucidate mechanisms behind defects in mitochondrial import pathways. Investigations using these models can reveal insights into the pathophysiology of conditions such as neurodegenerative diseases, metabolic syndromes, and mitochondrial myopathies. Furthermore, understanding the effects of TIMM17A depletion enhances our knowledge of cellular energy metabolism and apoptosis.

The scientific importance of TIMM17A Gene Knockout Cell Lines lies in their applications for both fundamental research and translational studies. They provide a platform for drug discovery efforts aimed at correcting mitochondrial dysfunctions and serve as valuable resources for assessing the impacts of genetic interventions on mitochondrial health. Compared to traditional models, these knockout cell lines offer specificity in studying the role of TIMM17A and can yield more relevant data regarding mitochondrial-related diseases.

Unique advantages of TIMM17A Gene Knockout Cell Lines include their reproducibility in experimental setups and the capacity for detailed phenotypic characterization. They can be effectively combined with CRISPR-Cas9 technology for further genetic manipulation, enhancing their utility in diverse experimental designs. Researchers and clinicians will find these cell lines invaluable for their ability to provide precise insights into mitochondrial function and related diseases.

Our company has years of expertise in developing high-quality biological products, ensuring that every TIMM17A Gene Knockout Cell Line is crafted with accuracy and reliability. We are committed to supporting researchers and clinicians in their quest for understanding and treating mitochondrial dysfunctions, reinforcing our position as a leader in the field of cellular and molecular biology.

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

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