Paper
18 May 2010 Raman microscopy of individual living human embryonic stem cells
S. M. Novikov, J. Beermann, S. I. Bozhevolnyi, L. M. Harkness, M. Kassem
Author Affiliations +
Abstract
We demonstrate the possibility of mapping the distribution of different biomolecules in living human embryonic stem cells grown on glass substrates, without the need for fluorescent markers. In our work we improve the quality of measurements by finding a buffer that gives low fluorescence, growing cells on glass substrates (whose Raman signals are relatively weak compared to that of the cells) and having the backside covered with gold to improve the image contrast under direct white light illumination. The experimental setup used for Raman microscopy is the commercially available confocal scanning Raman microscope (Alpha300R) from Witec and sub-μm spatially resolved Raman images were obtained using a 532 nm excitation wavelength.
© (2010) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
S. M. Novikov, J. Beermann, S. I. Bozhevolnyi, L. M. Harkness, and M. Kassem "Raman microscopy of individual living human embryonic stem cells", Proc. SPIE 7715, Biophotonics: Photonic Solutions for Better Health Care II, 771537 (18 May 2010); https://doi.org/10.1117/12.854207
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Cited by 1 scholarly publication.
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KEYWORDS
Raman spectroscopy

Microscopy

Stem cells

Confocal microscopy

Glasses

Luminescence

Image quality

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