Gene: UQCRHL
Official Full Name: ubiquinol-cytochrome c reductase hinge protein likeprovided by HGNC
Gene Summary: This gene has characteristics of a pseudogene derived from the UQCRH gene. However, there is still an open reading frame that could produce a protein of the same or nearly the same size as that of the UQCRH gene, so this gene is being called protein-coding for now. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO12772 | UQCRHL Knockout cell line (HeLa) | Human | UQCRHL | 1:3~1:6 | Negative | Online Inquiry |
KO12773 | UQCRHL Knockout cell line (HCT 116) | Human | UQCRHL | 1:2~1:4 | Negative | Online Inquiry |
KO12774 | UQCRHL Knockout cell line (A549) | Human | UQCRHL | 1:3~1:4 | Negative | Online Inquiry |
UQCRHL Gene Knockout Cell Lines are specialized cellular models designed to specifically disrupt the expression of the UQCRHL gene, which encodes for a subunit of the ubiquitous mitochondrial complex III in the electron transport chain. These knockout cell lines allow researchers to study the functional consequences of UQCRHL deficiency, thereby elucidating its role in cellular metabolism and oxidative phosphorylation processes.
The mechanism by which these cell lines operate involves the use of CRISPR-Cas9 technology to create targeted deletions or disruptions in the UQCRHL gene. By generating stable cell lines that lack UQCRHL expression, researchers can directly observe phenotypic changes and metabolic alterations resulting from impaired mitochondrial function. This provides critical insights into the pathophysiology of various diseases, including certain metabolic disorders and mitochondrial dysfunction syndromes.
The scientific importance of UQCRHL Gene Knockout Cell Lines extends to both basic and applied research. In a laboratory setting, these cell lines serve as invaluable tools for investigating the mitochondrial roles of UQCRHL in cell survival, apoptosis, and energy homeostasis. Clinically, understanding how UQCRHL contributes to disease mechanisms may lead to the identification of novel therapeutic targets, propelling advancements in treatments for conditions related to mitochondrial dysfunction.
Compared to conventional models, such as wild-type or overexpressing cell lines, UQCRHL Gene Knockout Cell Lines provide researchers with a unique and precise platform to dissect gene function in vitro. They eliminate variables associated with protein overexpression, allowing for more reliable data interpretation and experimental reproducibility.
For researchers and clinicians alike, these cell lines offer a critical advantage in the quest to understand mitochondrial biology and its implications in health and disease. By utilizing UQCRHL Gene Knockout Cell Lines, users can be at the forefront of mitochondrial research, leading to more effective therapeutic strategies.
Our company specializes in the development and distribution of cutting-edge gene editing tools and cellular models, ensuring researchers have access to high-quality products that can accelerate their discoveries in the ever-evolving field of molecular biology.
Please note that all services are for research use only. Not intended for any clinical use.
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