Real-time electrochemical detection of pathogen DNA using electrostatic interaction of a redox probe

The Analyst ◽  
2013 ◽  
Vol 138 (3) ◽  
pp. 907-915 ◽  
Author(s):  
Minhaz Uddin Ahmed ◽  
Sharifun Nahar ◽  
Mohammadali Safavieh ◽  
Mohammed Zourob
Nanoscale ◽  
2021 ◽  
Author(s):  
Carolina del Real Mata ◽  
Roozbeh Siavash Moakhar ◽  
Sayed Iman Isaac Hosseini ◽  
Mahsa Jalali ◽  
Sara Mahshid

Non-invasive liquid biopsies offer hope for a rapid, risk-free, real-time glimpse into cancer diagnostics. Recently, hydrogen peroxide (H2O2) is identified as a cancer biomarker due to continued release from cancer...


2019 ◽  
Vol 653 ◽  
pp. 1223-1230 ◽  
Author(s):  
J. Gallardo-Gonzalez ◽  
A. Baraket ◽  
S. Boudjaoui ◽  
T. Metzner ◽  
F. Hauser ◽  
...  

ACS Sensors ◽  
2018 ◽  
Vol 4 (1) ◽  
pp. 170-179 ◽  
Author(s):  
Olja Simoska ◽  
Marta Sans ◽  
Mignon D. Fitzpatrick ◽  
Christopher M. Crittenden ◽  
Livia S. Eberlin ◽  
...  

2020 ◽  
Vol 44 (25) ◽  
pp. 10604-10612
Author(s):  
Muthaiah Annalakshmi ◽  
Subbarayan Sumithra ◽  
Shen-Ming Chen ◽  
Tse-Wei Chen ◽  
Xuei-Hong Zheng

The highly sensitive real-time detection of antibiotic drugs (nitrofurantoin; NFT) has drawn significant research attention due to the extensive use of antibiotics, which may cause serious threats to environment as well as living things.


2008 ◽  
Vol 59 (12) ◽  
pp. 3407-3414 ◽  
Author(s):  
Angélique Besson-Bard ◽  
Sophie Griveau ◽  
Fethi Bedioui ◽  
David Wendehenne

2002 ◽  
Vol 92 (1) ◽  
pp. 112-116 ◽  
Author(s):  
L. M. Winton ◽  
J. K. Stone ◽  
L. S. Watrud ◽  
E. M. Hansen

Phaeocryptopus gaeumannii is a widespread foliar parasite of Douglas-fir. Although normally innocuous, the fungus also causes the defoliating disease Swiss needle cast in heavily infected needles. The extent of P. gaeumannii colonization in Douglas-fir foliage was estimated with real-time quantitative polymerase chain reaction (PCR) using TaqMan chemistry. In order to derive a normalized expression of colonization, both pathogen and host DNA were simultaneously amplified but individually detected by species-specific primers and TaqMan probes labeled with different fluorescent dyes. Detection of host DNA additionally provided an endogenous reference that served as both an internal positive control and adjusted for variation introduced by sample-to-sample differences in DNA extraction and PCR efficiencies. The genes employed for designing the TaqMan probes and primers were β-tubulin for the pathogen and a LEAFY/FLORICAULA-like gene involved in floral development for the tree host. Both probe/primer sets exhibited high precision and reproducibility over a linear range of 4 orders of magnitude. This eliminated the need to analyze samples in multiple dilutions when comparing lightly with heavily infected needles. Quantification of the fungus within needles was successful as early as 1 month after initial infection. Real-time PCR is the only method currently available to quantify P. gaeumannii colonization early in the first year of the colonization process.


Critical Care ◽  
2010 ◽  
Vol 14 (4) ◽  
pp. R159 ◽  
Author(s):  
Katsunori Yanagihara ◽  
Yuko Kitagawa ◽  
Masao Tomonaga ◽  
Kunihiro Tsukasaki ◽  
Shigeru Kohno ◽  
...  

2009 ◽  
Vol 24 (7) ◽  
pp. 2131-2136 ◽  
Author(s):  
Teh Huey Fang ◽  
Naveen Ramalingam ◽  
Dong Xian-Dui ◽  
Tan Swee Ngin ◽  
Zeng Xianting ◽  
...  

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