Gene: HADHA
Official Full Name: hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alphaprovided by HGNC
Gene Summary: This gene encodes the alpha subunit of the mitochondrial trifunctional protein, which catalyzes the last three steps of mitochondrial beta-oxidation of long chain fatty acids. The mitochondrial membrane-bound heterocomplex is composed of four alpha and four beta subunits, with the alpha subunit catalyzing the 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase activities. Mutations in this gene result in trifunctional protein deficiency or LCHAD deficiency. The genes of the alpha and beta subunits of the mitochondrial trifunctional protein are located adjacent to each other in the human genome in a head-to-head orientation. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO06423 | HADHA Knockout cell line (HeLa) | Human | HADHA | 1:3~1:6 | Negative | Online Inquiry |
KO06424 | HADHA Knockout cell line (HCT 116) | Human | HADHA | 1:2~1:4 | Negative | Online Inquiry |
KO06425 | HADHA Knockout cell line (HEK293) | Human | HADHA | 1:3~1:6 | Negative | Online Inquiry |
KO06426 | HADHA Knockout cell line (A549) | Human | HADHA | 1:3~1:4 | Negative | Online Inquiry |
HADHA Gene Knockout Cell Lines are specifically designed cellular models in which the HADHA gene has been inactivated, allowing for the detailed study of its biological functions, pathways, and role in metabolic disorders. These cell lines serve as powerful tools for researchers investigating the implications of HADHA gene mutations, which are linked to various lipid metabolism disorders, including primary mitochondrial diseases and complications associated with fatty acid oxidation.
The key mechanisms of these knockout cell lines involve the hereditary inactivation of the HADHA gene, leading to a disruption in the enzymatic activity responsible for mitochondrial fatty acid oxidation. By creating a controlled model that lacks this critical enzyme subunit, researchers can precisely observe the resulting metabolic pathways and dysfunctions that occur in its absence. This facilitates the exploration of the pathophysiology underlying metabolic diseases and opens avenues for the development of therapeutic interventions.
The scientific importance of HADHA Gene Knockout Cell Lines is underscored by their diverse applications in both research and clinical settings. These models are invaluable for drug screening, enabling the identification of potential compounds that may correct metabolic dysregulation. Moreover, they can be employed in gene therapy research, helping scientists to evaluate corrective strategies for restoring enzyme function.
Compared to conventional cell lines, HADHA Gene Knockout Cell Lines offer distinct advantages, such as greater specificity in modeling disease states and improved reproducibility in experimental outcomes. This specificity is essential for generating precise hypotheses about the role of the HADHA gene in metabolic processes, reducing the ambiguity found in non-targeted systems.
For researchers and clinicians involved in metabolic research or therapeutic development, HADHA Gene Knockout Cell Lines provide unparalleled insight into the mechanistic understanding of lipid metabolism disorders. Utilizing these cell lines can lead to groundbreaking discoveries, enhancing the prospect for novel treatment approaches.
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Please note that all services are for research use only. Not intended for any clinical use.
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