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UNG Knockout Cell Lines

Gene: UNG

Official Full Name: uracil DNA glycosylaseprovided by HGNC

Gene Summary: This gene encodes one of several uracil-DNA glycosylases. One important function of uracil-DNA glycosylases is to prevent mutagenesis by eliminating uracil from DNA molecules by cleaving the N-glycosylic bond and initiating the base-excision repair (BER) pathway. Uracil bases occur from cytosine deamination or misincorporation of dUMP residues. Alternative promoter usage and splicing of this gene leads to two different isoforms: the mitochondrial UNG1 and the nuclear UNG2. The UNG2 term was used as a previous symbol for the CCNO gene (GeneID 10309), which has been confused with this gene, in the literature and some databases. [provided by RefSeq, Nov 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO34843 UNG Knockout cell line (HeLa) Human UNG 1:3~1:6 Negative Online Inquiry
KO34844 UNG Knockout cell line (HCT 116) Human UNG 1:2~1:4 Negative Online Inquiry
KO34845 UNG Knockout cell line (HEK293) Human UNG 1:3~1:6 Negative Online Inquiry
KO34846 UNG Knockout cell line (A549) Human UNG 1:3~1:4 Negative Online Inquiry

Background

UNG Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to lack the uracil DNA glycosylase (UNG) gene. UNG plays a critical role in the base excision repair pathway by recognizing and excising uracil residues from DNA, which can arise from cytosine deamination. By utilizing these knockout cell lines, researchers can explore the biological consequences of UNG deficiency, including its impact on genomic stability, mutation rates, and response to various DNA-damaging agents.

The primary function of the UNG knockout cell lines is to serve as a tool for studying the role of UNG in DNA repair mechanisms and to better understand the implications of uracil incorporation into DNA. These cell lines allow scientists to delineate the pathways involved in maintaining DNA integrity, particularly in conditions that promote increased uracil incorporation, such as oxidative stress or certain viral infections. Furthermore, the absence of UNG provides a unique platform for examining tumorigenesis and the response to chemotherapeutic agents, potentially leading to novel therapeutic strategies that exploit the vulnerabilities associated with UNG deficiency.

The scientific importance of UNG knockout cell lines extends into various research and clinical applications, particularly in cancer biology, genetics, and virology. Researchers can leverage these models to investigate the roles of UNG in different cellular contexts, including its interactions with other repair proteins and its influence on mutation patterns in cancer cells.

Compared to alternative methods of studying uracil incorporation, such as pharmacological inhibition or transient knockdown approaches, these stable knockout cell lines offer reproducible, long-term models that facilitate comprehensive genetic and phenotypic analyses. This advantage leads to more reliable data and insights that can drive forward both basic research and clinical innovations.

For researchers and clinicians focusing on DNA repair mechanisms, cancer biology, or viral pathogenesis, our UNG Gene Knockout Cell Lines offer unparalleled value by providing a consistent, high-fidelity platform for inquiry. They not only deepen our understanding of fundamental biological processes but also hold the potential to uncover new therapeutic targets and strategies.

As a leader in the development of advanced biological research tools, our company prides itself on delivering high-quality genetic models that enhance scientific discovery and foster innovation in research and healthcare.

Please note that all services are for research use only. Not intended for any clinical use.

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