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E. Betzig, G. Patterson, R. Sougrat, O. Lindwasser, S. Olenych, J. Bonifacino, M. Davidson, J. Lippincott-Schwartz and H. Hess, “Imaging Intracellular Fluorescent Proteins at Nanometer Resolution,” Science, Vol. 313, No. 5379, 2006, pp. 1642-1645. doi:10.1126/science.1127344

has been cited by the following article:

• TITLE: A Low Cost and Versatile STED Superresolution Fluorescent Microscope

  AUTHORS: Daniel McBride, Chin Su, Jun Kameoka, Stanislav Vitha

  KEYWORDS: Stimulated Emission-Depletion Microscopy; STED

  JOURNAL NAME: Modern Instrumentation, Vol.2 No.3, July 12, 2013

  ABSTRACT: A versatile and inexpensive super-resolution fluorescent microscope that functions as easily as a conventional confocal microscope is described. Components of the microscope were designed on a platform which was placed atop a surplus microscope frame. All optical components and equipments used are given. The excitation and depletion beams are extracted from a compact low-cost supercontinuum light source. The focal spot of the depletion beam at the focal plane is studied and imaged by a 100 nm aperture near-field fiber tip. The collinear excitation and depletion beam focused by a 0.9 numerical aperture microscope objective produce a 90 nm lateral super-resolution as verified by imaging 100 nm diameter fluorescent beads.