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ERCC6 Knockout Cell Lines

Gene: ERCC6

Official Full Name: ERCC excision repair 6, chromatin remodeling factorprovided by HGNC

Gene Summary: This gene encodes a DNA-binding protein that is important in transcription-coupled excision repair. The encoded protein has ATP-stimulated ATPase activity, interacts with several transcription and excision repair proteins, and may promote complex formation at DNA repair sites. Mutations in this gene are associated with Cockayne syndrome type B and cerebrooculofacioskeletal syndrome 1. Alternative splicing occurs between a splice site from exon 5 of this gene to the 3' splice site upstream of the open reading frame (ORF) of the adjacent gene, piggyback-derived-3 (GeneID:267004), which activates the alternative polyadenylation site downstream of the piggyback-derived-3 ORF. The resulting transcripts encode a fusion protein that shares sequence with the product of each individual gene. [provided by RefSeq, Mar 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00514 ERCC6 knockout cell line (HEK293) Human ERCC6 1:3~1:6 Negative Online Inquiry
KO06044 ERCC6 Knockout cell line (HeLa) Human ERCC6 1:3~1:6 Negative Online Inquiry
KO06045 ERCC6 Knockout cell line (HCT 116) Human ERCC6 1:2~1:4 Negative Online Inquiry
KO06046 ERCC6 Knockout cell line (A549) Human ERCC6 1:3~1:4 Negative Online Inquiry

Background

ERCC6 Gene Knockout Cell Lines are specialized cellular models engineered to lack the expression of the ERCC6 gene, which encodes the protein vital for nucleotide excision repair (NER). This gene plays a critical role in the repair of DNA damage caused by various sources, including UV radiation and chemical mutagens. By utilizing these knockout cell lines, researchers can study the effects of impaired DNA repair mechanisms on cellular functions, thereby providing insights into the fundamental cellular processes involved in genomic stability, aging, and cancer development.

The key function of the ERCC6 gene knockout is to create a cellular environment that mimics the conditions found in certain genetic disorders, such as Cockayne syndrome, where defective DNA repair leads to pronounced developmental and neurodegenerative issues. The mechanism of action hinges on the complete ablation of the ERCC6 pathway, allowing for the observation of the compounded effects of DNA damage accumulation, which is essential in understanding how deficiencies in DNA repair contribute to pathologies.

The scientific importance of these cell lines is multifaceted; they are a powerful tool for elucidating the significance of the ERCC6 gene in cellular repair processes and for evaluating potential therapeutic interventions. In clinical research, they are used to screen for compounds that may enhance or restore NER function in affected cells, offering potential treatment strategies for DNA repair disorders.

One of the unique advantages of using ERCC6 gene knockout cell lines is their specificity. Unlike conventional cell lines that may still exhibit some level of ERCC6 activity, these knockout models provide a clear, unequivocal demonstration of the gene's absence, leading to more robust and reproducible results. Additionally, they serve as an unparalleled resource for drug development and validation in the realm of cancer therapy, as researchers can assess the effects of various treatments on cells lacking a critical repair mechanism.

For researchers and clinicians targeting nucleotide excision repair and its associated disorders, ERCC6 Gene Knockout Cell Lines represent an invaluable resource, facilitating deeper understanding and fostering innovative therapeutic solutions. Our company prides itself on delivering high-quality, rigorously validated biological products that empower the scientific community to advance research and improve clinical outcomes.

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

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