Gene: HADHB
Official Full Name: hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit betaprovided by HGNC
Gene Summary: This gene encodes the beta 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 beta subunit catalyzing the 3-ketoacyl-CoA thiolase activity. The encoded protein can also bind RNA and decreases the stability of some mRNAs. 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. Mutations in this gene result in trifunctional protein deficiency. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37424 | HADHB Knockout cell line (HeLa) | Human | HADHB | 1:3~1:6 | Negative | Online Inquiry |
KO37425 | HADHB Knockout cell line (HCT 116) | Human | HADHB | 1:2~1:4 | Negative | Online Inquiry |
KO37426 | HADHB Knockout cell line (HEK293) | Human | HADHB | 1:3~1:6 | Negative | Online Inquiry |
KO37427 | HADHB Knockout cell line (A549) | Human | HADHB | 1:3~1:4 | Negative | Online Inquiry |
HADHB Gene Knockout Cell Lines are advanced cellular models engineered to lack the HADHB gene, which encodes the mitochondrial enzyme, hydroxyacyl-CoA dehydrogenase, crucial for fatty acid metabolism. These knockout cell lines provide invaluable tools for elucidating the molecular mechanisms underlying lipid metabolism and its regulation, allowing researchers to explore the consequences of HADHB deficiency in detail.
The primary function of these cell lines is to enable the investigation of metabolic pathways involved in energy homeostasis and the implications of disrupted fatty acid oxidation. By utilizing CRISPR-Cas9 technology for the precise knockdown of the HADHB gene, these models are instrumental in studying the physiological and pathological effects of impaired mitochondrial function. Researchers can observe changes in substrate utilization, mitochondrial biogenesis, oxidative stress responses, and alterations in metabolic signaling pathways.
Scientifically, HADHB Gene Knockout Cell Lines have profound applications in both research and clinical settings, particularly in the context of metabolic disorders, mitochondrial diseases, and cancer metabolism. Their ability to mimic human disease states allows for enhanced understanding and potential therapeutic exploration, including gene therapy approaches, drug screening, and the assessment of novel metabolic modulators.
What differentiates our HADHB Gene Knockout Cell Lines from alternatives is the high specificity and efficiency of our knockout methodology, alongside confirmed genetic validation and comprehensive characterization. This ensures robustness and reproducibility, making them a reliable choice for researchers aiming to produce high-quality, scientifically sound data.
Researchers and clinicians will find substantial value in these cell lines as they facilitate deeper insights into the pathophysiological roles of HADHB, ultimately contributing to the development of targeted therapies and novel diagnostic tools. Our company, a leader in biological product innovation, is dedicated to advancing scientific research by providing expertly crafted models that reflect true biological relevance while maintaining rigorous quality standards.
Please note that all services are for research use only. Not intended for any clinical use.
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