نتایج جستجو برای: scanning electron micros

تعداد نتایج: 411390  

Journal: :Chinese Medical Journal 2007

Journal: :The Journal of biological chemistry 2007
Frank G M Wiertz Oliver-Matthias H Richter Bernd Ludwig Simon de Vries

The catalytic mechanism, electron transfer coupled to proton pumping, of heme-copper oxidases is not yet fully understood. Microsecond freeze-hyperquenching single turnover experiments were carried out with fully reduced cytochrome aa(3) reacting with O(2) between 83 micros and 6 ms. Trapped intermediates were analyzed by low temperature UV-visible, X-band, and Q-band EPR spectroscopy, enabling...

Journal: :Physical review letters 2007
Arzhang Ardavan Olivier Rival John J L Morton Stephen J Blundell Alexei M Tyryshkin Grigore A Timco Richard E P Winpenny

Using X-band pulsed electron-spin resonance, we report the intrinsic spin-lattice (T1) and phase-coherence (T2) relaxation times in molecular nanomagnets for the first time. In Cr7M heterometallic wheels, with M=Ni and Mn, phase-coherence relaxation is dominated by the coupling of the electron spin to protons within the molecule. In deuterated samples T2 reaches 3 micros at low temperatures, wh...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان فارس - دانشکده دندانپزشکی 1385

چکیده ندارد.

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Ding-Shyue Yang Omar F Mohammed Ahmed H Zewail

Progress has been made in the development of four-dimensional ultrafast electron microscopy, which enables space-time imaging of structural dynamics in the condensed phase. In ultrafast electron microscopy, the electrons are accelerated, typically to 200 keV, and the microscope operates in the transmission mode. Here, we report the development of scanning ultrafast electron microscopy using a f...

Journal: :Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention 2013
Raphael Sznitman Aurélien Lucchi Marco Cantoni Graham Knott Pascal Fua

Scanning Electron Microscopy (SEM) is an invaluable tool for biologists and neuroscientists to study brain structure at the intracellular level. While able to image tissue samples with up to 5 nm isotropic resolution, image acquisition is prohibitively slow and limits the size of processed samples. In this work, we propose a novel approach to speeding up imaging when looking for specific struct...

Journal: :iranian endodontic journal 0
saeed asgary department of endodontics, dental research center, dental school, shahid beheshti university of medical sciences, tehran, iran. [email protected] masoud parirokh department of endodontics, dental school, kerman university of medical sciences, kerman, iran mohammad jafar eghbal department of endodontics, dental research center, dental school, shahid beheshti university of medical sciences, tehran, iran jamileh ghoddusi department of endodontics, dental school, mashad university of medical sciences, mashad, iran

introduction: the purpose of this study was to evaluate the morphologic surface of gutta­percha cones after cutting with different methods. materials and methods: the apical 3 millimeters of forty standardized, gutta-percha cones size 40 were cut off using scissors or a scalpel against a glass slab. the samples were then examined under scanning electron microscopy (sem) for topographic deformit...

Journal: :Physical review letters 2008
S D Bergeson F Robicheaux

We present the first measurements and simulations of recombination fluorescence from ultracold neutral calcium plasmas. This method probes three-body recombination at times less than 1 micros, shorter than previously published time scales. For the lowest initial electron temperatures, the recombination rate scales with the density as n0(2.2), significantly slower than the predicted n0(3). Recom...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
P Wittung-Stafshede J C Lee J R Winkler H B Gray

Ferrocytochrome b562 [Fe(II)cyt b562] folding can be triggered by photoinduced electron transfer to unfolded Fe(III)cyt b562 in 2-3 M guanidine hydrochloride solutions. The folding rates increase with decreasing guanidine hydrochloride; the extrapolated time constant for this folding process in the absence of denaturant (5 micros) is near the predicted value for intrachain diffusion. The relati...

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