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ERCC1 Knockout Cell Lines

Gene: ERCC1

Official Full Name: ERCC excision repair 1, endonuclease non-catalytic subunitprovided by HGNC

Gene Summary: The product of this gene functions in the nucleotide excision repair pathway, and is required for the repair of DNA lesions such as those induced by UV light or formed by electrophilic compounds including cisplatin. The encoded protein forms a heterodimer with the XPF endonuclease (also known as ERCC4), and the heterodimeric endonuclease catalyzes the 5' incision in the process of excising the DNA lesion. The heterodimeric endonuclease is also involved in recombinational DNA repair and in the repair of inter-strand crosslinks. Mutations in this gene result in cerebrooculofacioskeletal syndrome, and polymorphisms that alter expression of this gene may play a role in carcinogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. The last exon of this gene overlaps with the CD3e molecule, epsilon associated protein gene on the opposite strand. [provided by RefSeq, Oct 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO04690 ERCC1 Knockout cell line (HeLa) Human ERCC1 1:3~1:6 Negative Online Inquiry
KO04691 ERCC1 Knockout cell line (HCT 116) Human ERCC1 1:2~1:4 Negative Online Inquiry
KO04692 ERCC1 Knockout cell line (HEK293) Human ERCC1 1:3~1:6 Negative Online Inquiry
KO04693 ERCC1 Knockout cell line (A549) Human ERCC1 1:3~1:4 Negative Online Inquiry

Background

ERCC1 Gene Knockout Cell Lines are specially engineered cellular models designed to investigate the function of the ERCC1 gene, which is integral to nucleotide excision repair (NER) – a key DNA repair pathway that influences cellular responses to DNA damage. These cell lines are derived from well-characterized backgrounds and are specifically modified to disrupt the ERCC1 gene, enabling researchers to study the implications of its absence on various cellular processes, including chromosomal stability, sensitivity to genotoxic agents, and overall cell viability.

The primary mechanism of action for ERCC1 involves its interaction with the excision repair cross-complementing group 1 protein (ERCC1-XPF), which forms a complex critical for the recognition and repair of bulky DNA lesions. By employing ERCC1 knockout cell lines, scientists can elucidate the role of ERCC1 in DNA repair mechanisms, understand its involvement in disease states such as cancer, and evaluate the efficacy of chemotherapeutic agents that cause DNA damage.

The scientific importance of these knockout cell lines extends beyond basic research; they hold significant applications in clinical settings for developing targeted therapies, understanding drug resistance, and predicting patient responses to oncological treatments. This makes ERCC1 Gene Knockout Cell Lines a valuable resource in personalized medicine, where the understanding of genetic mechanisms can lead to more tailored therapeutic strategies.

Unique selling points of these cell lines include their rigorous validation by molecular techniques to confirm knockout efficiency and the provision of comprehensive data regarding cellular behavior in comparison to wild-type controls. This validation ensures researchers can trust the models in their experiments, making comparability and reproducibility a cornerstone of their experimental design.

For researchers and clinicians alike, the value of ERCC1 Gene Knockout Cell Lines lies in their potential to drive breakthroughs in cancer research and therapy, providing insights that are crucial for advancing our understanding of DNA damage response pathways. Investing in these models allows for a closer examination of genetic contributions to oncogenesis, enhancing the overall efficacy of cancer treatment strategies.

Our company has extensive expertise in the development of advanced biological products, offering a range of meticulously characterized cell lines, which are tailored to meet the high standards required for cutting-edge research and clinical applications in the field of genetics and molecular biology.

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

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