Gene: NUBPL
Official Full Name: NUBP iron-sulfur cluster assembly factor, mitochondrialprovided by HGNC
Gene Summary: This gene encodes a member of the Mrp/NBP35 ATP-binding proteins family. The encoded protein is required for the assembly of the respiratory chain NADH dehydrogenase (complex I), an oligomeric enzymatic complex located in the inner mitochondrial membrane. Mutations in this gene cause mitochondrial complex I deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO26112 | NUBPL Knockout cell line (HeLa) | Human | NUBPL | 1:3~1:6 | Negative | Online Inquiry |
KO26113 | NUBPL Knockout cell line (HCT 116) | Human | NUBPL | 1:2~1:4 | Negative | Online Inquiry |
KO26114 | NUBPL Knockout cell line (HEK293) | Human | NUBPL | 1:3~1:6 | Negative | Online Inquiry |
KO26115 | NUBPL Knockout cell line (A549) | Human | NUBPL | 1:3~1:4 | Negative | Online Inquiry |
NUBPL Gene Knockout Cell Lines are genetically engineered cell lines in which the NUBPL gene has been selectively disrupted, enabling researchers to study the role of this gene in various biological processes. NUBPL, or Nuclear Uridine Triphosphate Biosynthesis 1, encodes a protein that is integral to mitochondrial respiratory function and DNA replication. By creating knockout versions of these cell lines, scientists can investigate the effects of NUBPL deficiency on cellular metabolism, mitochondrial function, and disease pathogenesis.
The key mechanism of action involves the use of CRISPR-Cas9 technology to achieve precise gene editing, allowing for the targeted deletion of the NUBPL gene. Researchers can then analyze how the absence of NUBPL affects cellular functions such as oxidative phosphorylation and energy production, providing insights into mitochondrial diseases and metabolic disorders. The distinct advantages of using NUBPL Gene Knockout Cell Lines over traditional models stem from their specificity and reproducibility, enabling more reliable data collection in experimental settings.
The scientific importance of these cell lines lies in their potential applications in fundamental research and therapeutic development. They serve as invaluable tools for understanding the underlying mechanisms of mitochondrial dysfunction and its contribution to various disorders, including neurodegenerative diseases and certain types of cancer. By offering a clear model for drug testing and gene therapy approaches, they position themselves as critical resources in translational medicine.
In comparison to alternative cell lines, NUBPL Gene Knockout Cell Lines provide a focused pathway to understanding disease mechanisms tied to mitochondrial function, thus offering researchers a powerful asset in their experimental arsenal. Their precise gene editing allows for nuanced studies that alternative models cannot replicate as effectively, ensuring robust experimental results.
With extensive expertise in genetic engineering and cell line development, our company is committed to providing high-quality biological tools that empower researchers and clinicians in their quest to advance scientific knowledge and therapies. Through our innovative offerings, we strive to support breakthroughs in mitochondrial research and beyond.
Please note that all services are for research use only. Not intended for any clinical use.
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