Gene: BRCC3
Official Full Name: BRCA1/BRCA2-containing complex subunit 3provided by HGNC
Gene Summary: This gene encodes a subunit of the BRCA1-BRCA2-containing complex (BRCC), which is an E3 ubiquitin ligase. This complex plays a role in the DNA damage response, where it is responsible for the stable accumulation of BRCA1 at DNA break sites. The component encoded by this gene can specifically cleave Lys 63-linked polyubiquitin chains, and it regulates the abundance of these polyubiquitin chains in chromatin. The loss of this gene results in abnormal angiogenesis and is associated with syndromic moyamoya, a cerebrovascular angiopathy. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 5. [provided by RefSeq, Jun 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO19378 | BRCC3 Knockout cell line (HeLa) | Human | BRCC3 | 1:3~1:6 | Negative | Online Inquiry |
KO19379 | BRCC3 Knockout cell line (HCT 116) | Human | BRCC3 | 1:2~1:4 | Negative | Online Inquiry |
KO19380 | BRCC3 Knockout cell line (HEK293) | Human | BRCC3 | 1:3~1:6 | Negative | Online Inquiry |
KO19381 | BRCC3 Knockout cell line (A549) | Human | BRCC3 | 1:3~1:4 | Negative | Online Inquiry |
BRCC3 Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to study the functions of the BRCC3 gene, which plays a critical role in DNA repair processes and cellular responses to stress. By employing CRISPR-Cas9 technology, these cell lines have been meticulously crafted to possess targeted deletions of the BRCC3 gene, facilitating an in-depth investigation into its biological functions and implications in various disease states, notably cancer and genomic instability.
These cell lines function primarily by mimicking the biological absence of the BRCC3 protein, thereby offering a unique platform for researchers to observe resultant cellular behavior and molecular changes. The knockout of BRCC3 alters pathways involved in homologous recombination repair, leading to a heightened sensitivity to DNA-damaging agents. Thus, researchers can utilize these cell lines to elucidate the role of BRCC3 in tumorigenesis, assess the efficacy of chemotherapeutic agents, and explore mechanisms of drug resistance.
The scientific importance of BRCC3 Gene Knockout Cell Lines extends to their applications in both basic research and translational medicine. Clinically, they offer insights into potential biomarkers for patient stratification and therapeutic targets in cancer treatment. Additionally, they can assist in understanding the intricacies of cellular responses during therapeutic interventions, ultimately contributing to personalized medicine approaches.
What sets these cell lines apart from alternatives is the precision of the gene knockout achieved through advanced gene-editing techniques, coupled with robust validation of knockout efficiency and phenotypic stability. This ensures reproducibility and reliability in experimental outcomes, making them superior for high-throughput screenings or mechanistic studies.
For researchers and clinicians, the BRCC3 Gene Knockout Cell Lines represent a valuable asset, providing essential tools for groundbreaking discoveries in cancer biology and therapeutic innovation. Our company, with extensive experience in the field of genetic engineering and cellular biology, stands committed to delivering high-quality biological products that enhance scientific inquiry and contribute to significant advancements in medicine.
Please note that all services are for research use only. Not intended for any clinical use.
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