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FEN1 Knockout Cell Lines

Gene: FEN1

Official Full Name: flap structure-specific endonuclease 1provided by HGNC

Gene Summary: The protein encoded by this gene removes 5' overhanging flaps in DNA repair and processes the 5' ends of Okazaki fragments in lagging strand DNA synthesis. Direct physical interaction between this protein and AP endonuclease 1 during long-patch base excision repair provides coordinated loading of the proteins onto the substrate, thus passing the substrate from one enzyme to another. The protein is a member of the XPG/RAD2 endonuclease family and is one of ten proteins essential for cell-free DNA replication. DNA secondary structure can inhibit flap processing at certain trinucleotide repeats in a length-dependent manner by concealing the 5' end of the flap that is necessary for both binding and cleavage by the protein encoded by this gene. Therefore, secondary structure can deter the protective function of this protein, leading to site-specific trinucleotide expansions. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
GP00313 FEN1 gRNA3-gRNA4 KO plasmid FEN1 $850
GP00314 FEN1 gRNA1-gRNA2 KO plasmid FEN1 $850
KO00132 FEN1 Knockout cell line (A549) Human FEN1 1:3~1:4 Negative Online Inquiry

Background

FEN1 Gene Knockout Cell Lines are specialized cellular systems that have been genetically engineered to lack the FEN1 (Flap Endonuclease 1) gene, which plays a crucial role in DNA replication and repair. These cell lines serve as vital tools for studying the fundamental biological processes involved in genome stability, cellular response to DNA damage, and the mechanisms underlying various diseases, particularly cancer. By uniquely eliminating the FEN1 gene, researchers can observe the phenotypic effects of this absence, including altered cellular growth, changes in apoptosis sensitivity, and defects in DNA repair mechanisms.

The primary function of FEN1 is to process DNA intermediates during the replication and repair processes, particularly in the removal of RNA primers and flap structures. Its knockout leads to the accumulation of unrepaired DNA damage, providing a critical insight into the cellular consequences of disrupted DNA repair pathways. These cell lines are invaluable in research settings, enabling scientists to elucidate the role of FEN1 in tumorigenesis, understand the biochemical pathways associated with genomic instability, and assess potential therapeutic targets for cancer treatment.

What sets FEN1 Gene Knockout Cell Lines apart from alternative models is their specificity and ability to mimic the biological relevance of FEN1 deficiency found in various cancers. Unlike general knockdown strategies, which may leave residual activity, these knockout lines exhibit a complete absence of FEN1, allowing for more precise analysis of its biological functions. Furthermore, they are compatible with numerous high-throughput screening applications, making them ideal for drug discovery and functional genomics.

The value of FEN1 Gene Knockout Cell Lines is significant for researchers and clinicians alike, as they provide an essential framework for exploring targeted therapies and understanding the molecular underpinnings of DNA repair-related diseases. By integrating these innovative tools into their research, scientists can accelerate advancements in therapeutic strategies aimed at enhancing genomic integrity.

Our company specializes in the development of advanced genetic tools and cellular models, ensuring high-quality products tailored to support cutting-edge research. Our expertise in this domain guarantees reliable and reproducible cellular systems, making them indispensable for advancing scientific knowledge and clinical applications.

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

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