Superresolution Structured Illumination Microscopy (SR-SIM)
ثبت نشده
چکیده
How Superresolution with ELYRA S.1 works The resolving power of a light microscope is limited to approximately 200nm in the lateral (XY) and 500nm in the axial (Z) direction. This so-called diffraction limit has been fi rst described by Ernst Abbe in 1873 (reference 1) and still holds true today. In simple terms, it posits that objects cannot be resolved with a conventional light microscope if their distance is less than half the wavelength of the light used for observation (Figure 1). In recent years, there have been several successful attempts to circumvent this problem and to achieve a resolution beyond the diffraction limit. In general, technologies with a resolving power exceeding the diffraction limit are nowadays collectively referred to as Superresolution Microscopy.
منابع مشابه
Ultrafast superresolution fluorescence imaging with spinning disk confocal microscope optics
Most current superresolution (SR) microscope techniques surpass the diffraction limit at the expense of temporal resolution, compromising their applications to live-cell imaging. Here we describe a new SR fluorescence microscope based on confocal microscope optics, which we name the spinning disk superresolution microscope (SDSRM). Theoretically, the SDSRM is equivalent to a structured illumina...
متن کاملLive Cell Imaging With Spatial Light Modulator-based Optical Sectioning Structured Illumination Microscopy
Structured illumination microscopy (SIM) is a method in fluorescence microscopy which works by acquiring a set of images using widefield detection. Each image in the set is made with a different position of an illumination mask, but with no mask in the detection path [1]. Subsequent image processing is used to produce an optically sectioned image (OS-SIM) [2 4], or an image with resolution beyo...
متن کاملSpeed limits of structured illumination microscopy.
A theoretical framework for widefield structured illumination microscopy (SIM) reconstruction from fewer than the commonly used nine raw frame acquisitions is introduced and applied in silico and in vitro. The proposed scheme avoids the recording of redundant spatial frequency components, which was necessary in previous SIM algorithms. This allows for gentler superresolution imaging at faster s...
متن کاملcsiLSFM combines light-sheet fluorescence microscopy and coherent structured illumination for a lateral resolution below 100 nm.
Light-sheet-based fluorescence microscopy (LSFM) features optical sectioning in the excitation process. It minimizes fluorophore bleaching as well as phototoxic effects and provides a true axial resolution. The detection path resembles properties of conventional fluorescence microscopy. Structured illumination microscopy (SIM) is attractive for superresolution because of its moderate excitation...
متن کاملSuperresolution microscopy for microbiology.
This review provides a practical introduction to superresolution microscopy from the perspective of microbiological research. Because of the small sizes of bacterial cells, superresolution methods are particularly powerful and suitable for revealing details of cellular structures that are not resolvable under conventional fluorescence light microscopy. Here we describe the methodological concep...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2010