Raman microscopy of individual living human embryonic stem cells

被引:1
作者
Novikov, S. M. [1 ]
Beermann, J. [1 ]
Bozhevolnyi, S. I. [1 ]
Harkness, L. M. [2 ]
Kassem, M. [2 ]
机构
[1] Univ So Denmark, Inst Sensors Signals & Electrotech, Niels Bohrs Alle 1, DK-5230 Odense M, Denmark
[2] Odense Univ Hosp, Dept Endocrinol, DK-5000 Odense, Denmark
来源
BIOPHOTONICS: PHOTONIC SOLUTIONS FOR BETTER HEALTH CARE II | 2010年 / 7715卷
关键词
Raman microscopy; Raman spectroscopy; confocal microscopy; vibrational imaging; Raman imaging;
D O I
10.1117/12.854207
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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-mu m spatially resolved Raman images were obtained using a 532 nm excitation wavelength.
引用
收藏
页数:5
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