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Fluorescence Recovery After Photobleaching (FRAP) of Fluorescence Tagged Proteins in Dendritic Spines of Cultured Hippocampal Neurons

机译:培养的海马神经元树突棘中荧光标记蛋白的光漂白(FRAP)后的荧光恢复。

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摘要

FRAP has been used to quantify the mobility of GFP-tagged proteins. Using a strong excitation laser, the fluorescence of a GFP-tagged protein is bleached in the region of interest. The fluorescence of the region recovers when the unbleached GFP-tagged protein from outside of the region diffuses into the region of interest. The mobility of the protein is then analyzed by measuring the fluorescence recovery rate. This technique could be used to characterize protein mobility and turnover rate.
机译:FRAP已用于定量GFP标签蛋白的迁移率。使用强激发激光,在目标区域中会漂白带有GFP标签的蛋白的荧光。当未漂白的,带有GFP标签的蛋白从区域外部扩散到目标区域时,该区域的荧光就会恢复。然后通过测量荧光回收率来分析蛋白质的迁移率。该技术可用于表征蛋白质的迁移率和周转率。

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