Gene: TP53BP1
Official Full Name: tumor protein p53 binding protein 1provided by HGNC
Gene Summary: This gene encodes a protein that functions in the DNA double-strand break repair pathway choice, promoting non-homologous end joining (NHEJ) pathways, and limiting homologous recombination. This protein plays multiple roles in the DNA damage response, including promoting checkpoint signaling following DNA damage, acting as a scaffold for recruitment of DNA damage response proteins to damaged chromatin, and promoting NHEJ pathways by limiting end resection following a double-strand break. These roles are also important during V(D)J recombination, class switch recombination and at unprotected telomeres. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO01998 | TP53BP1 Knockout cell line (HeLa) | Human | TP53BP1 | 1:3~1:6 | Negative | Online Inquiry |
KO01999 | TP53BP1 Knockout cell line (HCT 116) | Human | TP53BP1 | 1:2~1:4 | Negative | Online Inquiry |
KO02000 | TP53BP1 Knockout cell line (HEK293) | Human | TP53BP1 | 1:3~1:6 | Negative | Online Inquiry |
KO02001 | TP53BP1 Knockout cell line (A549) | Human | TP53BP1 | 1:3~1:4 | Negative | Online Inquiry |
TP53BP1 gene knockout cell lines are genetically engineered cell lines where the TP53BP1 gene has been deliberately inactivated. This product serves as an essential tool for researchers studying the role of TP53BP1 in cellular responses to DNA damage, tumor suppression, and cell cycle regulation. By disabling this key gene, researchers can circumvent mechanisms that would typically promote genomic stability, thereby allowing for more straightforward analysis of pathways related to cancer biology and therapeutic response.
The primary function of these knockout cell lines is to facilitate the investigation of TP53BP1's involvement in non-homologous end joining (NHEJ)—a critical pathway for repairing double-strand DNA breaks. The absence of TP53BP1 results in heightened sensitivity to DNA damaging agents, which can significantly affect cell survival, proliferation, and apoptosis, making it possible for researchers to elucidate the implications of TP53BP1 loss in various pathological contexts.
The scientific importance of TP53BP1 knockout cell lines extends beyond basic biology; they have practical applications in oncological studies, drug discovery, and the development of targeted therapies. By utilizing these cell lines, scientists can explore mechanisms of tumor resistance, enhance drug efficacy, and identify potential biomarkers for treatment response, thus contributing to personalized medicine.
Compared to traditional models, such as wild-type cell lines, TP53BP1 knockout cell lines offer a more precise environment to study the gene’s roles, without the confounding effects of normal TP53BP1 activity. This specificity enhances the reliability of experimental outcomes, allowing researchers to draw clearer conclusions about the gene's functions and interactions.
For researchers and clinicians alike, TP53BP1 knockout cell lines provide an unparalleled opportunity to advance our understanding of genomic integrity and its implications in cancer. These cell lines not only enrich experimental design but also empower scientists to translate their findings into potential clinical applications that can lead to improved patient outcomes.
With a commitment to innovation and excellence, our company specializes in providing high-quality biological products tailored to the needs of researchers in the field. We bring deep expertise in molecular biology, ensuring that our offerings, such as the TP53BP1 knockout cell lines, meet the rigorous standards required for cutting-edge scientific work.
Please note that all services are for research use only. Not intended for any clinical use.
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