Real-time, label-free isothermal solid-phase amplification/detection (ISAD) device for rapid detection of genetic alteration in cancers

Lab on a Chip ◽  
2013 ◽  
Vol 13 (11) ◽  
pp. 2106 ◽  
Author(s):  
Yong Shin ◽  
Agampodi Promoda Perera ◽  
Kyung Woo Kim ◽  
Mi Kyoung Park
Keyword(s):  
Real Time ◽  
Rapid Detection ◽  
Solid Phase ◽  
Genetic Alteration ◽  
Label Free

Real-time and label-free ring-resonator monitoring of solid-phase recombinase polymerase amplification

2015 ◽  
Vol 73 ◽  
pp. 130-137 ◽  
Author(s):  
Jonathan Sabaté del Río ◽  
Tim Steylaerts ◽  
Olivier Y.F. Henry ◽  
Peter Bienstman ◽  
Tim Stakenborg ◽  
...  
Keyword(s):  
Real Time ◽  
Ring Resonator ◽  
Solid Phase ◽  
Recombinase Polymerase Amplification ◽  
Label Free ◽  
Free Ring

Identification of hepatitis a virus in cell cultures by solid phase immune electron microscopy

1986 ◽  
Vol 44 ◽  
pp. 238-239
Author(s):  
C.D. Humphrey ◽  
T.L. Cromeans ◽  
E.H. Cook ◽  
D.W. Bradley
Keyword(s):  
Electron Microscopy ◽  
Liquid Phase ◽  
Cell Cultures ◽  
Rapid Detection ◽  
Hepatitis A ◽  
Hepatitis A Virus ◽  
Solid Phase ◽  
Immune Electron Microscopy ◽  
Detection And Identification

There is a variety of methods available for the rapid detection and identification of viruses by electron microscopy as described in several reviews. The predominant techniques are classified as direct electron microscopy (DEM), immune electron microscopy (IEM), liquid phase immune electron microscopy (LPIEM) and solid phase immune electron microscopy (SPIEM). Each technique has inherent strengths and weaknesses. However, in recent years, the most progress for identifying viruses has been realized by the utilization of SPIEM.

Rapid detection of Chlamydia/Chlamydophila group in samples collected from swine herds with and without reproductive disorders

2014 ◽  
Vol 17 (2) ◽  
pp. 367-369 ◽  
Author(s):  
K. Rypula ◽  
A. Kumala ◽  
P. Lis ◽  
K. Niemczuk ◽  
K. Płoneczka-Janeczko ◽  
...  
Keyword(s):  
Real Time ◽  
Real Time Pcr ◽  
Rapid Detection ◽  
Complement Fixation Test ◽  
Complement Fixation ◽  
Fixation Test ◽  
Reproductive Disorders ◽  
Serum Samples ◽  
Swine Herds

Abstract The study was carried out in seven reproductive herds of pigs. In three of them reproductive disorders were observed. Three herds consisted of 10-50 and four consisted of 120-500 adult sows and they were called small and medium, respectively. Fifty-seven adult sows were randomly selected from herds. Serum samples were tested using the complement fixation test and swabs from both eyes and from the vaginal vestibule were examined using real-time PCR. All serum samples were negative. Infected sows were present in each of the study herds. In total, there were 28 positive samples (53%, 28/48) in real-time PCR in sows with reproductive disorders and 35 (53%, 35/66) in sows selected from herds without problems in reproduction. One isolate proved to be Chlamydophila pecorum, whereas all the remaining were Chamydia suis

Rapid detection of OXA-23-like, OXA-24-like, and OXA-58-like carbapenemases from Acinetobacter species by real-time PCR

2020 ◽  
Vol 105 (4) ◽  
pp. 741-746
Author(s):  
M. Mentasti ◽  
K. Prime ◽  
K. Sands ◽  
S. Khan ◽  
M. Wootton
Keyword(s):  
Real Time ◽  
Real Time Pcr ◽  
Rapid Detection ◽  
Acinetobacter Species

scholarly journals Real‐Time and Label‐Free Measurement of Deubiquitinase Activity with a MspA Nanopore

ChemBioChem ◽  
2021 ◽  
Author(s):  
Spencer A. Shorkey ◽  
Jiale Du ◽  
Ryan Pham ◽  
Eric R. Strieter ◽  
Min Chen
Keyword(s):  
Real Time ◽  
Label Free
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