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首页> 外文期刊>Journal of Neuroscience Methods >Confocal microscopic imaging of fast UV-laser photolysis of caged compounds.
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Confocal microscopic imaging of fast UV-laser photolysis of caged compounds.

机译:笼状化合物的快速紫外激光光解的共聚焦显微镜成像。

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摘要

Using a pulsed UV laser in a confocal scanning microscope, we present a relatively cheap, accurate and efficient method for fast UV laser flash photolysis of caged molecules in two-dimensional cultured neurons. The laser light is introduced through the imaging optics, can be localized by a parallel red laser and can photolyse a sphere of less than 1 microm2, and evoke local fluorescence changes in the imaged neurons. Caged glutamate and caged fluorescein are used to illustrate a disparity between spines and their parent dendrites at a sub-micron resolution.
机译:在共聚焦扫描显微镜中使用脉冲UV激光,我们提出了一种相对便宜,准确和有效的方法,用于二维培养的神经元中笼状分子的快速UV激光快速光解。激光通过成像光学器件引入,可以被平行的红色激光定位,并且可以光解小于1 microm2的球体,并在成像的神经元中引起局部荧光变化。笼状谷氨酸盐和笼状荧光素用于说明亚微米分辨率下的棘突及其亲本树突之间的差异。

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