A facile method for coding and labeling assays on polystyrene beads with differently colored luminescent nanocrystals

2006 ◽  
Vol 384 (3) ◽  
pp. 645-650 ◽  
Author(s):  
J. Riegler ◽  
O. Ehlert ◽  
T. Nann
Author(s):  
Malcolm Brown ◽  
Reynolds M. Delgado ◽  
Michael J. Fink

While light microscopy has been used to image sub-micron objects, numerous problems with diffraction-limitations often preclude extraction of useful information. Using conventional dark-field and phase contrast light microscopy coupled with image processing, we have studied the following objects: (a) polystyrene beads (88nm, 264nm, and 557mn); (b) frustules of the diatom, Pleurosigma angulatum, and the T-4 bacteriophage attached to its host, E. coli or free in the medium. Equivalent images of the same areas of polystyrene beads and T-4 bacteriophages were produced using transmission electron microscopy.For light microscopy, we used a Zeiss universal microscope. For phase contrast observations a 100X Neofluar objective (N.A.=1.3) was applied. With dark-field, a 100X planachromat objective (N.A.=1.25) in combination with an ultra-condenser (N.A.=1.25) was employed. An intermediate magnifier (Optivar) was available to conveniently give magnification settings of 1.25, 1.6, and 2.0. The image was projected onto the back focal plane of a film or television camera with a Carl Zeiss Jena 18X Compens ocular.


2014 ◽  
Vol 2 (1) ◽  
Author(s):  
Hajime Arima ◽  
Hiroyuki Hirate ◽  
Takeshi Sugiura ◽  
Shugo Suzuki ◽  
Satoru Takahashi ◽  
...  

2007 ◽  
Vol 12 (5) ◽  
pp. 311-317 ◽  
Author(s):  
Vindhya Kunduru ◽  
Shalini Prasad

We demonstrate a technique to detect protein biomarkers contained in vulnerable coronary plaque using a platform-based microelectrode array (MEA). The detection scheme is based on the property of high specificity binding between antibody and antigen similar to most immunoassay techniques. Rapid clinical diagnosis can be achieved by detecting the amount of protein in blood by analyzing the protein's electrical signature. Polystyrene beads which act as transportation agents for the immobile proteins (antigen) are electrically aligned by application of homogenous electric fields. The principle of electrophoresis is used to produce calculated electrokinetic movement among the anti-C-reactive protein (CRP), or in other words antibody funtionalized polystyrene beads. The electrophoretic movement of antibody-functionalized polystyrene beads results in the formation of “Microbridges” between the two electrodes of interest which aid in the amplification of the antigen—antibody binding event. Sensitive electrical equipment is used for capturing the amplified signal from the “Microbridge” which essentially behaves as a conducting path between the two electrodes. The technique circumvents the disadvantages of conventional protein detection methods by being rapid, noninvasive, label-free, repeatable, and inexpensive. The same principle of detection can be applied for any receptor—ligand-based system because the technique is based only on the volume of the analyte of interest. Detection of the inflammatory coronary disease biomarker CRP is achieved at concentration levels spanning over the lower microgram/milliliter to higher order nanogram/milliliter ranges.


Langmuir ◽  
2005 ◽  
Vol 21 (10) ◽  
pp. 4262-4265 ◽  
Author(s):  
Bernd Zebli ◽  
Andrei S. Susha ◽  
Gleb B. Sukhorukov ◽  
Andrey L. Rogach ◽  
Wolfgang J. Parak

2015 ◽  
Vol 15 (12) ◽  
pp. 9879-9882 ◽  
Author(s):  
Wenyue Hou ◽  
Jing Xu ◽  
Xiuying Wang ◽  
Lifen Du ◽  
Chusen Huang ◽  
...  

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