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Rad51c Knockout Cell Lines

Gene: Rad51c

Official Full Name: RAD51 paralog Cprovided by MGI

Gene Summary: Enables crossover junction DNA endonuclease activity. Involved in telomere maintenance via recombination. Acts upstream of or within female meiosis sister chromatid cohesion; meiosis I; and spermatogenesis. Located in nucleus. Is expressed in several structures, including genitourinary system; heart; liver; lung; and spleen. Human ortholog(s) of this gene implicated in Fanconi anemia complementation group O and hereditary breast ovarian cancer syndrome. Orthologous to human RAD51C (RAD51 paralog C). [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
GP00332 Rad51c gRNA1-gRNA2 KO plasmid Rad51c $850
KO01115 Rad51c Knockout cell line(4T1) Mouse Rad51c 1:3~1:4 Negative Online Inquiry

Background

Rad51c Gene Knockout Cell Lines are genetically engineered cellular models specifically designed to study the function of the Rad51c gene, which plays a crucial role in DNA repair processes, particularly in homologous recombination. By disrupting the Rad51c gene's expression, these cell lines provide a powerful tool for researchers to investigate the dynamics of DNA damage response mechanisms and the implications of Rad51c deficiency in cancer biology.

The primary function of Rad51c involves facilitating the repair of double-strand breaks in DNA, which can be induced by various sources, including ionizing radiation and chemotherapeutic agents. The knockout of Rad51c leads to impaired homologous recombination repair pathways, making these cell lines indispensable for elucidating the consequences of DNA repair deficiencies. Researchers can utilize these models to study cellular responses to genotoxic stress, explore synthetic lethality in cancer therapy, and assess cellular survival and proliferation under conditions that simulate tumor microenvironments.

The scientific importance of Rad51c Gene Knockout Cell Lines is underscored by their diverse applications across research and clinical settings. These models enable in-depth investigations into genetic predispositions to cancers, especially breast and ovarian cancers associated with BRCA mutations. Furthermore, they serve as platforms to test novel therapeutic agents aimed at exploiting DNA repair deficiencies in cancer cells, providing valuable insights into personalized medicine approaches.

One of the unique selling points of the Rad51c Gene Knockout Cell Lines is their specificity and reliability compared to other models. Traditional methods of studying DNA repair often rely on pharmacological inhibitors that may have off-target effects. In contrast, these knockout cell lines provide a clean genetic background to accurately assess the functional impact of Rad51c loss in various experimental contexts.

For researchers and clinicians committed to advancing our understanding of cancer biology and developing innovative treatments, Rad51c Gene Knockout Cell Lines represent an invaluable resource. Their ability to mimic essential genetic alterations found in tumors while providing a controlled experimental environment enhances experimental reproducibility and relevance.

At [Your Company Name], we are committed to empowering researchers with high-quality biological products that are meticulously optimized for scientific inquiry. Our expertise in cellular models ensures that you receive products that not only meet high standards of validation but also drive discovery and innovation in the realm of molecular biology.

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

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