Abstract
Heme proteins, such as hemoglobins and cytochromes, play important roles in various biological processes. Here we employ the two-photon excited photothermal effect as a contrast mechanism to map heme proteins distribution. Particularly, both a thermal lens scheme and a high-frequency modulation are utilized to enhance the signal-to-noise ratio. We demonstrate label-free imaging of individual red blood cells, subcellular distribution of cytochromes in live mammalian cells, and the microvascular networks in mouse ear tissue and in a zebrafish gill. © 2010 American Institute of Physics.
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CITATION STYLE
Lu, S., Min, W., Chong, S., Holtom, G. R., & Xie, X. S. (2010). Label-free imaging of heme proteins with two-photon excited photothermal lens microscopy. Applied Physics Letters, 96(11). https://doi.org/10.1063/1.3308485
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