scholarly journals Multiplex Detection of Nucleic Acids Using Recombinase Polymerase Amplification and a Molecular Colorimetric 7-Segment Display

ACS Omega ◽  
2019 ◽  
Vol 4 (7) ◽  
pp. 11388-11396 ◽  
Author(s):  
Jia Li ◽  
Nina M. Pollak ◽  
Joanne Macdonald
Lab on a Chip ◽  
2015 ◽  
Vol 15 (13) ◽  
pp. 2759-2766 ◽  
Author(s):  
Friedrich Schuler ◽  
Frank Schwemmer ◽  
Martin Trotter ◽  
Simon Wadle ◽  
Roland Zengerle ◽  
...  

Centrifugal step emulsification enables dead volume free emulsification, it was applied to the first digital droplet recombinase polymerase amplification (RPA).


2012 ◽  
Vol 50 (10) ◽  
pp. 3208-3215 ◽  
Author(s):  
C. Ohrmalm ◽  
R. Eriksson ◽  
M. Jobs ◽  
M. Simonson ◽  
M. Stromme ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (4) ◽  
pp. e0153359 ◽  
Author(s):  
Zhao Li ◽  
Yong Liu ◽  
Qingquan Wei ◽  
Yuanjie Liu ◽  
Wenwen Liu ◽  
...  

2011 ◽  
Vol 83 (9) ◽  
pp. 3533-3540 ◽  
Author(s):  
Feng Shen ◽  
Elena K. Davydova ◽  
Wenbin Du ◽  
Jason E. Kreutz ◽  
Olaf Piepenburg ◽  
...  

2014 ◽  
Vol 50 (29) ◽  
pp. 3824-3826 ◽  
Author(s):  
Qing Wang ◽  
Hui Wang ◽  
Xiaohai Yang ◽  
Kemin Wang ◽  
Fang Liu ◽  
...  

A simple assay for multiplex DNA detection has been developed using a low cost microfluidic chip and a personal glucose meter.


2021 ◽  
Author(s):  
Jingyan Lin ◽  
Yunxia Wu ◽  
Ronghua Yang ◽  
Jingru Wang ◽  
Wenjie Wu ◽  
...  

Abstract Background: Circulating tumor nucleic acids (CTNAs) have been employed as the potential marker for tumor diagnosis and management, which are highly related to the tumorigenesis, progression and metastasis processes. Therefore, it is of significance to develop a highly-sensitive and reliable methods for detection of CTNAs, especially the multiplex point mutation detection of blood-derived CTNAs. Results: Herein, a gold island-enhanced multiplex quantum dots (QDs) fluorescent platform was constructed for highly-sensitive detection of CTNAs in serum. The gold island-enhanced multiplex fluorescent strategy was designed as the highly-efficient signal giving-out mode which could amplify the fluorescence of QDs, realized a homogeneous nano-platform for the enrichment, multiplex detection and point mutations monitoring of CTNAs with the principle of base-stacking. A high sensitivity of 10 amol and desirable specificity were achieved, and the performance index for analysis of clinical CTNAs samples indicated that the gold island-enhanced multiplex QDs fluorescent strategy could realize multiplex point mutations detection of CTNAs in complex blood samples. Conclusions: Hence, this platform achieved high detection rate in clinical samples that suitably met the clinical-requirements for multiplex detection and point mutations monitoring of CTNAs, and thus has the potential to serve as the tumor liquid biopsy strategy based on CTNAs.


Author(s):  
Norman Davidson

The basic protein film technique for mounting nucleic acids for electron microscopy has proven to be a general and powerful tool for the working molecular biologist in characterizing different nucleic acids. It i s possible to measure molecular lengths of duplex and single-stranded DNAs and RNAs. In particular, it is thus possible to as certain whether or not the nucleic acids extracted from a particular source are or are not homogeneous in length. The topological properties of the polynucleotide chain (linear or circular, relaxed or supercoiled circles, interlocked circles, etc. ) can also be as certained.


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