Gene: PARP1
Official Full Name: poly(ADP-ribose) polymerase 1provided by HGNC
Gene Summary: This gene encodes a chromatin-associated enzyme, poly(ADP-ribosyl)transferase, which modifies various nuclear proteins by poly(ADP-ribosyl)ation. The modification is dependent on DNA and is involved in the regulation of various important cellular processes such as differentiation, proliferation, and tumor transformation and also in the regulation of the molecular events involved in the recovery of cell from DNA damage. In addition, this enzyme may be the site of mutation in Fanconi anemia, and may participate in the pathophysiology of type I diabetes. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00541 | PARP1 knockout cell line (HeLa) | Human | PARP1 | 1:3~1:6 | Negative | Online Inquiry |
KO00661 | PARP1 Knockout cell line(HCT 116) | Human | PARP1 | 1:2~1:4 | Negative | Online Inquiry |
KO01001 | PARP1 Knockout cell line (A549) | Human | PARP1 | 1:3~1:4 | Negative | Online Inquiry |
KO09476 | PARP1 Knockout cell line (HEK293) | Human | PARP1 | 1:3~1:6 | Negative | Online Inquiry |
PARP1 Gene Knockout Cell Lines are genetically engineered cell lines that have been specifically modified to disrupt the Parp1 gene, which encodes the enzyme poly(ADP-ribose) polymerase 1 (PARP1). This enzyme plays a crucial role in DNA repair processes and cellular responses to genomic stress. By creating these knockout cell lines, researchers can effectively study the implications of PARP1 absence on various cellular functions, including DNA damage response, intracellular signaling, and overall cell viability.
The principal mechanism behind PARP1's function involves its activity in detecting DNA single-strand breaks and facilitating their repair through the recruitment of repair proteins, thereby enhancing cell survival following genotoxic stress. By observing PARP1 knockout models, scientists can elucidate the contributions of this enzyme in tumorigenesis, drug resistance, and the efficacy of PARP inhibitors, which are increasingly utilized in therapeutic settings for cancers harboring homologous recombination deficiencies.
The scientific relevance of PARP1 Gene Knockout Cell Lines extends across both fundamental biological research and clinical applications. These cell lines serve as invaluable tools for investigating cancer biology, molecular pathways involved in therapeutic responses, and the development of novel pharmacological interventions. Their existence aids in understanding how cells cope with DNA damage and can provide insight into personalized medicine approaches for cancer treatment.
One of the significant advantages of using PARP1 knockout cell lines is their ability to mimic physiological conditions where PARP1 activity is absent, offering a unique vantage point over traditional models. Compared to alternative systems, such as siRNA-mediated knockdown, these stable knockout lines offer more reliable, long-term studies by minimizing off-target effects and providing consistent results.
Researchers and clinicians looking to enhance their studies on DNA repair mechanisms and therapeutic vulnerabilities will find PARP1 Gene Knockout Cell Lines to be essential. These models not only facilitate groundbreaking research but also pave the way for innovative strategies in cancer treatment, thereby having a substantial impact on patient care.
At [Your Company Name], our expertise lies in developing high-quality, genetically modified cell lines that meet rigorous scientific standards. Our commitment to advancing research and clinical applications ensures that our products remain at the forefront of biological innovation.
Please note that all services are for research use only. Not intended for any clinical use.
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