Gene: GCDH
Official Full Name: glutaryl-CoA dehydrogenaseprovided by HGNC
Gene Summary: The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 12. [provided by RefSeq, Mar 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37701 | GCDH Knockout cell line (HeLa) | Human | GCDH | 1:3~1:6 | Negative | Online Inquiry |
KO37702 | GCDH Knockout cell line (HCT 116) | Human | GCDH | 1:2~1:4 | Negative | Online Inquiry |
KO37703 | GCDH Knockout cell line (HEK293) | Human | GCDH | 1:3~1:6 | Negative | Online Inquiry |
KO37704 | GCDH Knockout cell line (A549) | Human | GCDH | 1:3~1:4 | Negative | Online Inquiry |
GCDH Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to lack the function of the GCDH (glutaryl-CoA dehydrogenase) gene. This gene plays a crucial role in the catabolism of certain amino acids and is essential for the degradation of glutaryl-CoA, a metabolite implicated in several metabolic disorders. By creating GCDH knockout models, researchers can study the biochemical pathways associated with GCDH deficiency, including the resulting accumulation of toxic metabolites and their physiological effects.
The key function of these knockout cell lines lies in their ability to mimic the metabolic dysfunctions seen in conditions such as glutaric aciduria type I. By observing the cellular responses and alterations in metabolic profiles in these lines, scientists can gain valuable insights into disease mechanisms and potential therapeutic targets. These cell lines serve as a powerful platform for both basic research and drug development, facilitating the exploration of novel enzymatic pathways and therapeutic interventions.
From a scientific perspective, the GCDH Gene Knockout Cell Lines hold significant relevance in both experimental research and clinical applications. They offer researchers the opportunity to investigate the impact of GCDH deficiency on cellular metabolism, neuron development, and overall cellular physiology, thereby advancing our understanding of metabolic disorders.
One of the primary advantages of these cell lines over alternative models is their specificity and relevance to human pathology, as they closely mimic a genuine genetic deficiency. Additionally, these knockout lines are easy to maintain in culture, allowing for high-throughput experimentation, which is essential for drug screening and biomarker identification.
For researchers and clinicians alike, GCDH Gene Knockout Cell Lines are an invaluable tool for uncovering the intricacies of metabolic diseases. Their unique genetic profile makes them an ideal model for studying disease progression and the efficacy of potential treatments, contributing crucial data that can lead to improved patient outcomes.
With years of expertise in cell line development and a commitment to advancing biomedical research, our company is dedicated to providing high-quality biological products that empower researchers to make significant strides in their work.
Please note that all services are for research use only. Not intended for any clinical use.
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