High Visibility of Atom Wave Interferometer Based on the Ideal Atom Beam Splitter

Author(s):  
A.S. Pazgalev ◽  
Y.V. Rozhdestvensky
Keyword(s):  
2000 ◽  
Vol 25 (18) ◽  
pp. 1382 ◽  
Author(s):  
Dirk Müller ◽  
Eric A. Cornell ◽  
Marco Prevedelli ◽  
Peter D. D. Schwindt ◽  
Alex Zozulya ◽  
...  

2006 ◽  
Author(s):  
S. V. Borisenok ◽  
Yu. D. Selishcheva ◽  
Yu. V. Rozhdestvensky

2003 ◽  
Vol 68 (3) ◽  
Author(s):  
A. Zh. Muradyan ◽  
A. A. Poghosyan ◽  
P. R. Berman
Keyword(s):  

2006 ◽  
Vol 74 (2) ◽  
Author(s):  
Naceur Gaaloul ◽  
Annick Suzor-Weiner ◽  
Laurence Pruvost ◽  
Mourad Telmini ◽  
Eric Charron

2000 ◽  
Vol 85 (26) ◽  
pp. 5543-5546 ◽  
Author(s):  
Olivier Houde ◽  
Demascoth Kadio ◽  
Laurence Pruvost
Keyword(s):  

2021 ◽  
Author(s):  
Ingo Gregor ◽  
Eugenia Butkevich ◽  
Joerg Enderlein ◽  
Soheil Mojiri

One of the most widely used microscopy techniques in biology and medicine is fluorescence microscopy, offering high specificity in labeling as well as maximum sensitivity. For live cell imaging, the ideal fluorescence microscope should offer high spatial resolution, fast image acquisition, three-dimensional sectioning, and multi-color detection. However, most existing fluorescence microscopes have to compromise between these different requirements. Here, we present a multi-plane multi-color wide-field microscope that uses a dedicated beam-splitter for recording volumetric data in eight focal planes and for three emission colors with frame rates of hundreds of volumes per second. We demonstrate the efficiency and performance of our system by three-dimensional imaging of multiply labeled fixed and living cells.


2004 ◽  
Vol 70 (6) ◽  
Author(s):  
A. Zh. Muradyan ◽  
G. A. Muradyan ◽  
P. R. Berman

2016 ◽  
Vol 25 (8) ◽  
pp. 080311
Author(s):  
Xiaojun Jiang ◽  
Xiaolin Li ◽  
Haichao Zhang ◽  
Yuzhu Wang
Keyword(s):  

Author(s):  
M.S. Shahrabadi ◽  
T. Yamamoto

The technique of labeling of macromolecules with ferritin conjugated antibody has been successfully used for extracellular antigen by means of staining the specimen with conjugate prior to fixation and embedding. However, the ideal method to determine the location of intracellular antigen would be to do the antigen-antibody reaction in thin sections. This technique contains inherent problems such as the destruction of antigenic determinants during fixation or embedding and the non-specific attachment of conjugate to the embedding media. Certain embedding media such as polyampholytes (2) or cross-linked bovine serum albumin (3) have been introduced to overcome some of these problems.


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