The blinking phenomena of the quantum dots have been utilized in the super-resolution localization microscopy to map out the locations of individual quantum dots on a total internal reflection microscope. Our result indicated that the reconstructed image of quantum dots agreed with the topographic image measured by atomic force microscopy. Because of the superior optical properties of the quantum dots, the high localization resolution can be achieved in the shorter acquisition time with larger detected photon numbers. When the cells were labeled with quantum dots, the sub-cellular structures could be clearly seen in the reconstructed images taken by a commercial microscope without using complicated optical systems, special photo-switchable dye pairs or photo-activated fluorescence proteins.
机构:
Univ Colorado, Boulder, CO 80309 USA
JILA, Natl Inst Stand & Technol, Boulder, CO USA
Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USAUniv Colorado, Boulder, CO 80309 USA
Fomenko, Vasiliy
;
Nesbitt, David J.
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机构:
Univ Colorado, Boulder, CO 80309 USA
JILA, Natl Inst Stand & Technol, Boulder, CO USA
Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USAUniv Colorado, Boulder, CO 80309 USA
机构:
Univ Colorado, Boulder, CO 80309 USA
JILA, Natl Inst Stand & Technol, Boulder, CO USA
Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USAUniv Colorado, Boulder, CO 80309 USA
Fomenko, Vasiliy
;
Nesbitt, David J.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Colorado, Boulder, CO 80309 USA
JILA, Natl Inst Stand & Technol, Boulder, CO USA
Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USAUniv Colorado, Boulder, CO 80309 USA