Optical multichannel detection system suitable for a Fabry–Perot interferometer

1984 ◽  
Vol 55 (2) ◽  
pp. 153-157 ◽  
Author(s):  
J. Fünfschilling ◽  
M. Brūlhart ◽  
H. R. Hidber ◽  
I. Zschokke‐Gränacher
2000 ◽  
Vol 71 (2) ◽  
pp. 522-529 ◽  
Author(s):  
Emmanuil Rabinovich ◽  
Michael J. O’Brien ◽  
Steven R. J. Brueck ◽  
Gabriel P. Lopez

2016 ◽  
Author(s):  
Julia Wecker ◽  
Andreas Bauch ◽  
Steffen Kurth ◽  
Gauri Mangalgiri ◽  
Markus Gaitzsch ◽  
...  

1997 ◽  
Vol 8 (4) ◽  
pp. 449-452 ◽  
Author(s):  
Matthias Seel ◽  
Eberhard Wildermuth ◽  
Wolfgang Zinth

2000 ◽  
Author(s):  
Emmanuil M. Rabinovich ◽  
Michael J. O'Brien II ◽  
Steven R. J. Brueck ◽  
S. Yang ◽  
Victor H. Perez-Luna ◽  
...  

2000 ◽  
Vol 3 (2) ◽  
pp. 93-99 ◽  
Author(s):  
ROBIN L. STEARS ◽  
ROBERT C. GETTS ◽  
STEVEN R. GULLANS

Stears, Robin L., Robert C. Getts, and Steven R. Gullans. A novel, sensitive detection system for high-density microarrays using dendrimer technology. Physiol Genomics 3: 93–99, 2000.—To improve signal detection on cDNA microarrays, we adapted a fluorescent oligonucleotide dendrimeric signal amplification system to microarray technology. This signal detection method requires 16-fold less RNA for probe synthesis, does not depend on the incorporation of fluorescent dNTPs into a reverse transcription reaction, generates a high signal-to-background ratio, and can be used to allow for multichannel detection on a single chip. Furthermore, since the dendrimers can be detected individually, it may be possible, by employing dendrimer-binding standards, to calculate the numbers of bound cDNAs can be estimated. These features make the dendrimer signal detection reagent ideal for high-throughput functional genomics research.


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