Gene: GAPDH
Official Full Name: glyceraldehyde-3-phosphate dehydrogenaseprovided by HGNC
Gene Summary: This gene encodes a member of the glyceraldehyde-3-phosphate dehydrogenase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The product of this gene catalyzes an important energy-yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde-3-phosphate in the presence of inorganic phosphate and nicotinamide adenine dinucleotide (NAD). The encoded protein has additionally been identified to have uracil DNA glycosylase activity in the nucleus. Also, this protein contains a peptide that has antimicrobial activity against E. coli, P. aeruginosa, and C. albicans. Studies of a similar protein in mouse have assigned a variety of additional functions including nitrosylation of nuclear proteins, the regulation of mRNA stability, and acting as a transferrin receptor on the cell surface of macrophage. Many pseudogenes similar to this locus are present in the human genome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
GP00173 | GAPDH gRNA3-gRNA4 KO plasmid | GAPDH | $850 | |||
GP00350 | GAPDH gRNA1-gRNA2 KO plasmid | GAPDH | $850 | |||
KO00579 | GAPDH Knockout cell line(A549) | Human | GAPDH | 1:3~1:4 | Negative | Online Inquiry |
GAPDH Gene Knockout Cell Lines are genetically engineered cell lines in which the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene has been inactivated, providing researchers with a powerful tool for studying the biological roles of this enzyme and its involvement in various metabolic pathways. GAPDH is traditionally known for its critical function in glycolysis; however, it also plays essential roles in processes such as cellular signaling, apoptosis, and gene expression regulation. By creating a knockout model, scientists can elucidate the compensatory mechanisms that occur in its absence, thereby deepening our understanding of cellular metabolism and its dysregulation in diseases.
The key function of these cell lines is their ability to facilitate experimental study of residual metabolic pathways, gene interactions, and downstream effects of GAPDH knockouts. Researchers can employ these models in various assays including metabolic flux analysis, cell proliferation studies, and drug response evaluations to investigate the role of GAPDH in disease states such as cancer, diabetes, and neurodegeneration.
The scientific importance of GAPDH Gene Knockout Cell Lines is highlighted by their utility in both basic and applied research settings. They are particularly valuable for the development of new therapeutic strategies, as the biological implications of GAPDH in pathophysiology are gaining traction in the research community.
Compared to alternatives, these knockout cell lines offer several distinct advantages. They are specifically engineered for reproducibility and predictability in experimental outcomes, allowing for clearer data interpretation. Additionally, the precise nature of gene knockout technology ensures a complete and effective loss of function, while maintaining the integrity of cellular architecture, which can be a limitation in partial inhibition studies.
For researchers and clinicians, the value of GAPDH Knockout Cell Lines lies in their ability to provide insights into metabolic regulation and disease mechanisms, paving the way for innovative treatment approaches. Our company combines extensive expertise in genetic engineering with a commitment to high-quality biological products to offer reliable and effective solutions for your research needs. By choosing our GAPDH Gene Knockout Cell Lines, you are investing in a tool that propels your scientific inquiry forward with confidence and precision.
Please note that all services are for research use only. Not intended for any clinical use.
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