Gene: HMGCL
Official Full Name: 3-hydroxy-3-methylglutaryl-CoA lyaseprovided by HGNC
Gene Summary: The protein encoded by this gene belongs to the HMG-CoA lyase family. It is a mitochondrial enzyme that catalyzes the final step of leucine degradation and plays a key role in ketone body formation. Mutations in this gene are associated with HMG-CoA lyase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37330 | HMGCL Knockout cell line (HeLa) | Human | HMGCL | 1:3~1:6 | Negative | Online Inquiry |
KO37331 | HMGCL Knockout cell line (HCT 116) | Human | HMGCL | 1:2~1:4 | Negative | Online Inquiry |
KO37332 | HMGCL Knockout cell line (HEK293) | Human | HMGCL | 1:3~1:6 | Negative | Online Inquiry |
KO37333 | HMGCL Knockout cell line (A549) | Human | HMGCL | 1:3~1:4 | Negative | Online Inquiry |
HMGCL Gene Knockout Cell Lines refer to genetically engineered cell lines in which the hydroxymethylglutaryl-CoA lyase (HMGCL) gene has been functionally disrupted. HMGCL is crucial for the metabolism of certain amino acids and ketone bodies, playing a vital role in the synthesis of acetoacetate and the metabolic pathway of isoprenoids. By creating cell lines with the HMGCL gene knocked out, researchers can investigate the consequences of this genetic alteration on cellular metabolism, function, and associated pathological conditions.
The mechanism behind these knockout cell lines utilizes advanced CRISPR/Cas9 gene-editing technology, allowing for precise and efficient inactivation of the HMGCL gene. This approach provides researchers with stable, reproducible models to study metabolic disorders such as HMG-CoA lyase deficiency, which can result in hypoglycemia, ketoacidosis, and neurological dysfunction. These models serve not only to understand disease mechanisms but also to identify potential therapeutic targets and screening compounds.
The scientific importance of HMGCL Gene Knockout Cell Lines extends to applications in both research and clinical settings. They offer valuable insights into metabolic pathways, facilitate the testing of metabolic drug candidates, and support the development of gene therapy approaches. Compared to traditional cell lines, these knockout models provide a more refined environment to explore the specific impacts of HMGCL dysfunction without confounding factors often present in wild-type strains.
The advantages of using HMGCL Gene Knockout Cell Lines include their ability to mirror the metabolic anomalies seen in human disease, thereby enhancing the validity of research findings. This focus on precise genetic manipulation allows researchers to produce significant, replicable results and to tailor experimental designs to their specific needs.
For researchers and clinicians seeking to advance their understanding of metabolic disorders and explore innovative treatment avenues, HMGCL Gene Knockout Cell Lines represent an unparalleled resource. Our company specializes in the development of high-quality genetic models and is committed to empowering the scientific community with products that facilitate groundbreaking research. By leveraging our expertise, users can enhance their discoveries and contribute significantly to the field of metabolic disease research.
Please note that all services are for research use only. Not intended for any clinical use.
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