Gene: DCLRE1B
Official Full Name: DNA cross-link repair 1Bprovided by HGNC
Gene Summary: DNA interstrand cross-links prevent strand separation, thereby physically blocking transcription, replication, and segregation of DNA. DCLRE1B is one of several evolutionarily conserved genes involved in repair of interstrand cross-links (Dronkert et al., 2000 [PubMed 10848582]).[supplied by OMIM, Mar 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20275 | DCLRE1B Knockout cell line (HeLa) | Human | DCLRE1B | 1:3~1:6 | Negative | Online Inquiry |
KO20276 | DCLRE1B Knockout cell line (HCT 116) | Human | DCLRE1B | 1:2~1:4 | Negative | Online Inquiry |
KO20277 | DCLRE1B Knockout cell line (HEK293) | Human | DCLRE1B | 1:3~1:6 | Negative | Online Inquiry |
DCLRE1B Gene Knockout Cell Lines are specialized human cell lines engineered to disrupt the DCLRE1B gene, which encodes a critical enzyme involved in DNA repair pathways. These knockout models are pivotal for studying the role of DCLRE1B in cellular responses to genotoxic stress, as well as its implications in oncogenesis and genomic stability. By employing CRISPR-Cas9 or other gene editing technologies, these cell lines enable researchers to elucidate the functional outcomes of DCLRE1B deficiency, leading to comprehensive insights into its biological significance.
The primary mechanism utilized in the DCLRE1B knockout approach involves the precise deletion of the DCLRE1B coding sequence, resulting in the complete loss of function of the encoded enzyme. This deficiency can then be assessed in various assays to evaluate effects on DNA damage repair, cell cycle progression, and apoptosis. Importantly, DCLRE1B is known to play a role in the repair of double-strand DNA breaks, and understanding its knockdown can significantly advance our knowledge of cellular resilience or vulnerability to different therapeutic agents.
In both research and clinical settings, these knockout cell lines serve as invaluable tools for investigating DNA repair mechanisms and developing new therapeutic strategies for cancer treatment, particularly in tumors exhibiting compromised DNA repair capabilities. Researchers can leverage these cell lines to identify potential drug targets, assess the off-target effects of chemotherapeutic agents, and explore the interplay between genetic deficiencies and drug resistance.
Compared to traditional methods of gene expression modulation, such as RNA interference, the DCLRE1B knockout cell lines provide a more stable and complete disruption of gene function. This genetic permanence allows for more profound and reproducible insight into cellular mechanisms over time, thus enhancing the reliability of experimental data.
For researchers and clinicians focused on genetic, cancer, and therapeutic investigations, DCLRE1B Gene Knockout Cell Lines represent a cutting-edge product that can significantly streamline experimental workflows and elucidate complex biological questions. Our company prides itself on its commitment to providing high-quality biological products, along with extensive expertise in gene editing technologies, ensuring that our customers receive reliable and innovative tools for advancing their research objectives.
Please note that all services are for research use only. Not intended for any clinical use.
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