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ERCC8 Knockout Cell Lines

Gene: ERCC8

Official Full Name: ERCC excision repair 8, CSA ubiquitin ligase complex subunitprovided by HGNC

Gene Summary: This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO38534 ERCC8 Knockout cell line (HeLa) Human ERCC8 1:3~1:6 Negative Online Inquiry
KO38535 ERCC8 Knockout cell line (HCT 116) Human ERCC8 1:2~1:4 Negative Online Inquiry
KO38536 ERCC8 Knockout cell line (HEK293) Human ERCC8 1:3~1:6 Negative Online Inquiry
KO38537 ERCC8 Knockout cell line (A549) Human ERCC8 1:3~1:4 Negative Online Inquiry

Background

ERCC8 Gene Knockout Cell Lines are genetically modified cell lines in which the ERCC8 gene has been specifically disrupted or "knocked out." The ERCC8 gene encodes a protein that is pivotal in the nucleotide excision repair (NER) pathway, which plays a vital role in the cellular response to DNA damage, particularly from UV radiation and chemical mutagens. By using these knockout cell lines, researchers can study the effects of the absence of the ERCC8 protein on cellular behavior, DNA repair mechanisms, and overall genomic stability.

These cell lines function as invaluable tools for dissecting the molecular pathways underlying DNA repair processes. When the ERCC8 gene is knocked out, the resultant cells exhibit deficiencies in NER, leading to increased sensitivity to DNA-damaging agents. This enables researchers to elucidate the role of ERCC8 in tumorigenesis, aging, and various skin disorders, as well as to explore potential therapeutic strategies targeting NER defects.

Scientifically, ERCC8 knockout cell lines have broad applications in research aimed at understanding genetic diseases associated with defective DNA repair, such as Xeroderma Pigmentosum. In clinical settings, they offer potential avenues for drug development and testing, allowing scientists to model and target the pathways that become dysregulated when NER is compromised.

One of the critical advantages of our ERCC8 Gene Knockout Cell Lines is their high fidelity and reproducibility, providing researchers with consistent and reliable data. Unlike simpler models, these knockout lines closely mimic human cellular responses, making them superior for translational research. Additionally, our product is validated for use in numerous experimental setups, thus ensuring researchers the flexibility to investigate myriad biological questions without compromising rigor.

The value of our ERCC8 Gene Knockout Cell Lines extends beyond basic research; they are essential for translational applications that could lead to advancements in cancer therapy, regenerative medicine, and personalized medicine approaches. With deep expertise in genetic engineering and cell biology, our company is committed to supplying innovative biological products that empower researchers and clinicians to unlock new scientific discoveries and therapeutic strategies.

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

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