Gene: NMNAT3
Official Full Name: nicotinamide nucleotide adenylyltransferase 3provided by HGNC
Gene Summary: This gene encodes a member of the nicotinamide/nicotinic acid mononucleotide adenylyltransferase family. These enzymes use ATP to catalyze the synthesis of nicotinamide adenine dinucleotide or nicotinic acid adenine dinucleotide from nicotinamide mononucleotide or nicotinic acid mononucleotide, respectively. The encoded protein is localized to mitochondria and may also play a neuroprotective role as a molecular chaperone. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO15697 | NMNAT3 Knockout cell line (HCT 116) | Human | NMNAT3 | 1:2~1:4 | Negative | Online Inquiry |
KO15698 | NMNAT3 Knockout cell line (HEK293) | Human | NMNAT3 | 1:3~1:6 | Negative | Online Inquiry |
KO15699 | NMNAT3 Knockout cell line (A549) | Human | NMNAT3 | 1:3~1:4 | Negative | Online Inquiry |
NMNAT3 Gene Knockout Cell Lines are advanced research tools specifically designed to facilitate the study of the NAD+ biosynthetic pathway and its implications in various biological processes. NMNAT3 encodes the enzyme nicotinamide mononucleotide adenylyltransferase 3, crucial for the synthesis of NAD+, a cofactor involved in critical cellular functions including energy metabolism, DNA repair, and cell signaling. By creating knockout cell lines deficient in NMNAT3, researchers can effectively elucidate the cellular mechanisms affected by alterations in NAD+ metabolism, providing insights into metabolic disorders, neurodegenerative diseases, and the aging process.
The unique functionality of NMNAT3 Gene Knockout Cell Lines lies in their ability to serve as experimental models that mimic pathological conditions associated with aberrant NAD+ levels. These cell lines demonstrate altered rates of apoptosis, cellular proliferation, and metabolic regulation, allowing researchers to investigate the downstream effects of NMNAT3 deficiency in a controlled environment. The precise genetic engineering applied to generate these knockout lines ensures that the findings are specific and relevant to the NMNAT3 gene, reducing the background noise often encountered in standard cell line studies.
From a scientific standpoint, NMNAT3 knockout models are invaluable in preclinical research and drug development. They provide a platform to test potential therapeutics targeting NAD+ metabolism, contributing to the search for effective treatments for age-related diseases, diabetes, and neurological disorders. Their ability to replicate human cellular responses enhances translational research efforts, making them essential for drug efficacy and safety assessments.
What distinguishes NMNAT3 Gene Knockout Cell Lines from alternative models is their robust and reproducible performance, which ensures consistent results across experiments. They are available with extensive characterizations validated by gene editing techniques such as CRISPR-Cas9, granting researchers confidence in their experimental design. In an era where precision medicine is paramount, employing these knockout cell lines ensures that researchers and clinicians conduct studies that are both relevant and impactful.
Our company is dedicated to advancing biological research, offering high-quality reagents and tools like NMNAT3 Gene Knockout Cell Lines, backed by years of expertise in genomic engineering and a commitment to supporting the scientific community's mission to uncover the complexities of human biology.
Please note that all services are for research use only. Not intended for any clinical use.
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