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EARS2 Knockout Cell Lines

Gene: EARS2

Official Full Name: glutamyl-tRNA synthetase 2, mitochondrialprovided by HGNC

Gene Summary: This gene encodes a member of the class I family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of glutamate to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 12 (COXPD12). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO28042 EARS2 Knockout cell line (HeLa) Human EARS2 1:3~1:6 Negative Online Inquiry
KO28043 EARS2 Knockout cell line (HCT 116) Human EARS2 1:2~1:4 Negative Online Inquiry
KO28044 EARS2 Knockout cell line (HEK293) Human EARS2 1:3~1:6 Negative Online Inquiry
KO28045 EARS2 Knockout cell line (A549) Human EARS2 1:3~1:4 Negative Online Inquiry

Background

EARS2 Gene Knockout Cell Lines are specially engineered cellular models that feature targeted deletion of the EARS2 gene, which encodes for mitochondrial glutamyl-tRNA synthetase. This gene plays a critical role in mitochondrial protein synthesis by catalyzing the binding of glutamate to its corresponding tRNA. The knockout model allows for the precise investigation of gene function, pathogenic mechanisms, and therapeutic interventions related to various mitochondrial disorders.

Key functions of EARS2 Gene Knockout Cell Lines include elucidating the effects of disrupted mitochondrial protein synthesis on cellular metabolism and viability. By creating a loss-of-function scenario, researchers can observe altering phenotypes that are representative of mitochondrial dysfunction, enhancing our understanding of metabolic pathways and their implications in disease. This model serves as an invaluable tool in both fundamental research concerning mitochondrial biology and translational studies aimed at developing therapies for mitochondrial-related diseases.

The scientific importance of EARS2 knockout models extends into the realm of clinical applications, as they facilitate the study of conditions such as encephalopathy and cardiomyopathy associated with mitochondrial dysfunction. Through this model, researchers can explore novel drug candidates, enabling the development of targeted treatments that may restore mitochondrial function, thus advancing clinical science.

What sets EARS2 Gene Knockout Cell Lines apart from conventional models is their ability to provide nuanced insights into gene function that cannot be replicated through alternative approaches, such as siRNA-mediated knockdown, which often leads to incomplete gene silencing. These knockout lines provide a robust and stable platform for experimentation, minimizing variability and improving reproducibility across experiments.

For researchers and clinicians focusing on mitochondrial biology, the value of EARS2 Gene Knockout Cell Lines lies in the potential for groundbreaking discoveries and translational advancements that could lead to innovative therapeutic strategies. By utilizing these advanced cell lines, scientists can accelerate their research trajectories, thereby enhancing the prospects for improved patient outcomes.

Our company is dedicated to advancing biological research through high-quality, innovative products and services, and our EARS2 Gene Knockout Cell Lines exemplify our commitment to enhancing the scientific community's understanding of complex genetic and cellular processes.

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

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