Gene: ALDH18A1
Official Full Name: aldehyde dehydrogenase 18 family member A1provided by HGNC
Gene Summary: This gene is a member of the aldehyde dehydrogenase family and encodes a bifunctional ATP- and NADPH-dependent mitochondrial enzyme with both gamma-glutamyl kinase and gamma-glutamyl phosphate reductase activities. The encoded protein catalyzes the reduction of glutamate to delta1-pyrroline-5-carboxylate, a critical step in the de novo biosynthesis of proline, ornithine and arginine. Mutations in this gene lead to hyperammonemia, hypoornithinemia, hypocitrullinemia, hypoargininemia and hypoprolinemia and may be associated with neurodegeneration, cataracts and connective tissue diseases. Alternatively spliced transcript variants, encoding different isoforms, have been described for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00495 | ALDH18A1 Knockout cell line (HEK293) | Human | ALDH18A1 | 1:3~1:6 | Negative | Online Inquiry |
KO03540 | ALDH18A1 Knockout cell line (HeLa) | Human | ALDH18A1 | 1:3~1:6 | Negative | Online Inquiry |
KO03541 | ALDH18A1 Knockout cell line (HCT 116) | Human | ALDH18A1 | 1:2~1:4 | Negative | Online Inquiry |
KO03542 | ALDH18A1 Knockout cell line (A549) | Human | ALDH18A1 | 1:3~1:4 | Negative | Online Inquiry |
ALDH18A1 Gene Knockout Cell Lines represent a sophisticated tool in molecular biology that facilitates the study of the aldehyde dehydrogenase 18 family member A1 gene (ALDH18A1) and its associated biological functions. These cell lines have been genetically modified to disrupt the ALDH18A1 gene, thereby allowing researchers to investigate the consequences of its absence on cellular processes. This technique enables the elucidation of gene function, signaling pathways, and metabolic networks in a controlled environment.
The knockout mechanism relies on CRISPR-Cas9 or similar genome editing technologies, precisely targeting and disrupting the ALDH18A1 gene to produce a loss-of-function phenotype. This model is particularly valuable for exploring the role of ALDH18A1 in cellular metabolism, oxidative stress response, and potential implications in disease states like cancer and metabolic disorders. Understanding the pathways influenced by this gene may provide significant insights into therapeutic targets and biomarker discovery.
The scientific importance of ALDH18A1 Gene Knockout Cell Lines extends to various applications, including drug screening, metabolic research, and functional genomics. They offer a significant advantage over conventional models, providing more relevant human-like responses and enabling researchers to study the direct effects of ALDH18A1 perturbations in vitro. Compared to alternative models, these knockout lines allow for a clearer understanding of gene function without the confounding effects of other genetic variables.
For researchers and clinicians, the value of ALDH18A1 Gene Knockout Cell Lines lies in their capacity to accelerate discoveries in biomedical research and drug development. By providing a robust system to dissect gene function, these cell lines can lead to novel insights into metabolic regulation and disease mechanisms. This can ultimately guide the development of targeted therapies and improve patient outcomes.
With a commitment to innovation and excellence, our company specializes in developing high-quality genetic models and cell lines tailored for advanced research needs. Leverage our expertise to enhance your understanding of ALDH18A1 and drive your research forward.
Please note that all services are for research use only. Not intended for any clinical use.
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