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ERCC6L Knockout Cell Lines

Gene: ERCC6L

Official Full Name: ERCC excision repair 6 like, spindle assembly checkpoint helicaseprovided by HGNC

Gene Summary: This gene encodes a member of the SWItch/Sucrose Non-Fermentable (SWI/SNF2) family of proteins, and contains a SNF2-like ATPase domain and a PICH family domain. One distinguishing feature of this SWI/SNF protein family member is that during interphase, the protein is excluded from the nucleus, and only associates with chromatin after the nuclear envelope has broken down. This protein is a DNA translocase that is thought to bind double-stranded DNA that is exposed to stretching forces, such as those exerted by the mitotic spindle. This protein associates with ribosomal DNA and ultra-fine DNA bridges (UFBs), fine structures that connect sister chromatids during anaphase at some sites such as fragile sites, telomeres and centromeres. This gene is required for the faithful segregation of sister chromatids during mitosis, and the ATPase activity of this protein required for the resolution of UFBs before cytokinesis. [provided by RefSeq, May 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00200 ERCC6L Knockout cell line (HeLa) Human ERCC6L 1:3~1:6 Negative Online Inquiry
KO20581 ERCC6L Knockout cell line (HCT 116) Human ERCC6L 1:2~1:4 Negative Online Inquiry
KO20582 ERCC6L Knockout cell line (HEK293) Human ERCC6L 1:3~1:6 Negative Online Inquiry
KO20583 ERCC6L Knockout cell line (A549) Human ERCC6L 1:3~1:4 Negative Online Inquiry

Background

ERCC6L Gene Knockout Cell Lines are genetically engineered cell models designed to facilitate the study of the ERCC6L gene, a vital component involved in DNA repair mechanisms, particularly in the context of nucleotide excision repair (NER). By utilizing CRISPR-Cas9 technology, these knockout cell lines have been meticulously created to eliminate the function of the ERCC6L gene, allowing researchers to observe the resultant phenotypic changes and understand the gene's role in cellular processes, including DNA damage response, cell cycle regulation, and genomic stability.

The key mechanism of these cell lines revolves around their ability to mimic the loss of ERCC6L gene activity, providing a platform for functional assays that measure the impact on DNA repair pathways. This includes assessing sensitivity to DNA-damaging agents, analyzing cell viability, and examining alterations in gene expression profiles. By enabling such investigations, ERCC6L Gene Knockout Cell Lines can elucidate the pathways involved in genetic disorders related to DNA repair deficiencies.

Scientifically, these cell lines hold tremendous importance in both research and clinical settings. They serve as invaluable tools for studying various conditions associated with compromised DNA repair mechanisms such as genetic diseases, aging-related degeneration, and cancer. Specifically, they can aid in identifying potential therapeutic targets and biomarkers for clinical interventions.

The unique selling points of ERCC6L Gene Knockout Cell Lines lie in their high specificity and reproducibility, ensuring reliable data that is critical for advancing scientific understanding. Compared to alternative models, such as transient knockdowns, these stable knockout lines provide consistent experimental conditions over time, facilitating longitudinal studies and enabling a deeper insight into temporal dynamics of the cellular response to DNA damage.

For researchers and clinicians, the value of using ERCC6L Gene Knockout Cell Lines is substantial. They pave the way for groundbreaking discoveries in genetic research, improving targeted therapies, and providing a robust model for pharmaceutical testing that could ultimately enhance patient outcomes.

Our company brings extensive expertise in genetic engineering and cell line development, ensuring that our products meet the highest scientific standards. We are committed to providing researchers with cutting-edge tools that empower innovative discoveries in the realm of genetics and cellular biology.

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

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