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The accumulation of p53 protein in response to DNA damage in vitro is well established and appears to induce growth arrest and apoptosis by the transcriptional regulation of other genes. In irradiated mice, p53 protein accumulates in splenocytes, thymocytes and osteocytes, though not in hepatocytes. Mouse T3T3 cells express high levels of phenotypically characteristic wild type p53 protein which carries two missense mutations. The range of antigenic sites in mouse p53 protein and human p53 protein is very similar.
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