Gene: ERCC5
Official Full Name: ERCC excision repair 5, endonucleaseprovided by HGNC
Gene Summary: This gene encodes a single-strand specific DNA endonuclease that makes the 3' incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G), which is also referred to as xeroderma pigmentosum VII (XP7), a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, cognitive disability, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene. [provided by RefSeq, Feb 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37974 | ERCC5 Knockout cell line (HeLa) | Human | ERCC5 | 1:3~1:6 | Negative | Online Inquiry |
KO37975 | ERCC5 Knockout cell line (HCT 116) | Human | ERCC5 | 1:2~1:4 | Negative | Online Inquiry |
KO37976 | ERCC5 Knockout cell line (HEK293) | Human | ERCC5 | 1:3~1:6 | Negative | Online Inquiry |
KO37977 | ERCC5 Knockout cell line (A549) | Human | ERCC5 | 1:3~1:4 | Negative | Online Inquiry |
ERCC5 Gene Knockout Cell Lines are genetically modified cells specifically designed to lack expression of the ERCC5 gene, which encodes a crucial protein involved in the nucleotide excision repair (NER) pathway. This repair mechanism is vital for maintaining genomic stability by correcting DNA damage inflicted by environmental factors such as UV radiation and chemical mutagens. By utilizing these knockout cell lines, researchers have a powerful tool to investigate the role of ERCC5 in DNA repair processes and understand the molecular mechanisms underlying cellular responses to genotoxic stress.
The primary function of ERCC5 knockout cell lines lies in their ability to provide a controlled environment where the absence of the ERCC5 protein can elucidate the pathways affected by its loss. With the lack of functional ERCC5, these cell lines exhibit a marked increase in susceptibility to DNA damage and reduced cellular viability upon exposure to DNA-damaging agents. This unique characteristic allows for the exploration of compensatory repair mechanisms and the identification of potential therapeutic targets, especially in cancer cells where NER pathways often become dysregulated.
In research and clinical applications, ERCC5 knockout cell lines are invaluable for studying various aspects of cancer biology, including tumorigenesis, resistance to chemotherapy, and the development of personalized medicine strategies. They provide critical insights into the genetic and biochemical defects associated with certain cancer types, contributing to the development of targeted therapies that can improve patient outcomes.
Compared to traditional cell lines, ERCC5 gene knockout cell lines offer specificity and precision that enhance experimental reproducibility. Their unique status allows researchers to ascertain the effects of specific drugs or genetic modifications in a manner that approximates human pathophysiological conditions.
For researchers and clinicians engaged in cancer research, molecular biology, or pharmacogenomics, the value of ERCC5 Gene Knockout Cell Lines is evident. They enable the development of innovative therapeutic strategies and facilitate discoveries that can lead to breakthroughs in the treatment and understanding of various diseases.
Our company specializes in the production of tailored genetic models, leveraging our expertise in gene editing technologies to deliver products like the ERCC5 Gene Knockout Cell Lines that support cutting-edge research and clinical advancements.
Please note that all services are for research use only. Not intended for any clinical use.
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