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ACO1 Knockout Cell Lines

Gene: ACO1

Official Full Name: aconitase 1provided by HGNC

Gene Summary: The protein encoded by this gene is a bifunctional, cytosolic protein that functions as an essential enzyme in the TCA cycle and interacts with mRNA to control the levels of iron inside cells. When cellular iron levels are high, this protein binds to a 4Fe-4S cluster and functions as an aconitase. Aconitases are iron-sulfur proteins that function to catalyze the conversion of citrate to isocitrate. When cellular iron levels are low, the protein binds to iron-responsive elements (IREs), which are stem-loop structures found in the 5' UTR of ferritin mRNA, and in the 3' UTR of transferrin receptor mRNA. When the protein binds to IRE, it results in repression of translation of ferritin mRNA, and inhibition of degradation of the otherwise rapidly degraded transferrin receptor mRNA. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Alternative splicing results in multiple transcript variants [provided by RefSeq, Jan 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO02648 ACO1 Knockout cell line (HeLa) Human ACO1 1:3~1:6 Negative Online Inquiry
KO02649 ACO1 Knockout cell line (HCT 116) Human ACO1 1:2~1:4 Negative Online Inquiry
KO02650 ACO1 Knockout cell line (HEK293) Human ACO1 1:3~1:6 Negative Online Inquiry
KO02651 ACO1 Knockout cell line (A549) Human ACO1 1:3~1:4 Negative Online Inquiry

Background

ACO1 Gene Knockout Cell Lines are specifically engineered cellular models that have had the ACO1 gene, also known as the aconitase 1 gene, disrupted or entirely knocked out. This gene plays a critical role in the cellular response to iron and is involved in the regulation of iron homeostasis and mitochondrial function. By creating ACO1 knockout cell lines, researchers can investigate the effects of the absence of this gene on cellular metabolism, iron-sulfur cluster biogenesis, and overall mitochondrial health.

The key functions of these knockout cell lines hinge on their ability to provide insights into the cellular consequences of ACO1 deficiency. Without ACO1, cells exhibit altered iron metabolism, leading to potential dysregulation of metabolic pathways and increased oxidative stress. Researchers utilize these models to dissect the mechanisms underlying iron deficiency anemia, mitochondrial diseases, and various neurodegenerative conditions.

Scientifically, ACO1 Gene Knockout Cell Lines hold significant importance in both basic research and clinical applications. They serve as vital tools for studying disease mechanisms, drug responses, and therapeutic interventions targeting mitochondrial dysfunction and metabolic dysregulation. Their application spans a wide array of fields, including oncology, neurobiology, and hematology, making them indispensable to the development of novel therapies and diagnostics.

One of the primary advantages of our ACO1 knockout line is the precision of the knockout technique employed, which ensures a clean genetic modification with minimal off-target effects. This high degree of specificity enables researchers to obtain reliable data, ultimately enhancing the reproducibility of experiments. Comparatively, traditional methods often lead to incomplete knockouts or variable expression levels, which can complicate data interpretation.

For researchers, clinicians, and pharmaceutical developers, investing in ACO1 Gene Knockout Cell Lines processes significant value. Their capacity to mimic disease states and provide a platform for screening candidate therapies accelerates translational research efforts. Furthermore, with our company’s extensive expertise in gene editing and cellular model development, we ensure the highest quality standards in our products, making our ACO1 knockout lines a leading choice for advancing scientific discovery.

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

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