The distribution of BrKα/RbKα peak intensity ratio in human whole blood samples

1994 ◽  
Vol 42 (3) ◽  
pp. 231-241 ◽  
Author(s):  
C. Shenberg ◽  
S. Spiegel ◽  
S. Chaitchik ◽  
P. Jordan ◽  
M. Kitzis ◽  
...  
2021 ◽  
Vol 2 (1) ◽  
pp. 100311
Author(s):  
Daniella C. Terenzi ◽  
Ehab Bakbak ◽  
Justin Z. Trac ◽  
Mohammad Al-Omran ◽  
Adrian Quan ◽  
...  

2014 ◽  
Vol 436 ◽  
pp. 72-77 ◽  
Author(s):  
Li-Ting Liao ◽  
Chi-Chih Liao ◽  
Chiu-Ching Liu ◽  
Ting-Ya Yang ◽  
Giueng-Chueng Wang

2011 ◽  
Vol 412 (23-24) ◽  
pp. 2150-2156 ◽  
Author(s):  
Ming-Song Hsieh ◽  
Tai-Guang Wu ◽  
Chein-Shyong Su ◽  
Wen-Jing Cheng ◽  
Namik Ozbek ◽  
...  

2015 ◽  
Vol 51 (64) ◽  
pp. 12748-12751 ◽  
Author(s):  
Yuhui Wang ◽  
Kai Jiang ◽  
Jiali Zhu ◽  
Ling Zhang ◽  
Hengwei Lin

A novel FRET model employing fluorescent carbon dots and MnO2nanosheets as donor–acceptor pairs is built for GSH sensing.


2011 ◽  
Vol 3 (10) ◽  
pp. 652-660 ◽  
Author(s):  
Martin Schönfelder ◽  
Hande Hofmann ◽  
Patricia Anielski ◽  
Detlef Thieme ◽  
Renate Oberhoffer ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Paolo Gaibani ◽  
Mara Mariconti ◽  
Gloria Bua ◽  
Sonia Bonora ◽  
Davide Sassera ◽  
...  

Molecular methods are important tools in the diagnosis of bloodstream bacterial infections, in particular in patients treated with antimicrobial therapy, due to their quick turn-around time. Here we describe a new broad-range real-time PCR targeting the 23S rDNA gene and capable to detect as low as 10 plasmid copies per reaction of targeted bacterial 23S rDNA gene. Two commercially available DNA extraction kits were evaluated to assess their efficiency for the extraction of plasma and whole blood samples spiked with different amount of eitherStaphylococcus aureusorEscherichia coli, in order to find the optimal extraction method to be used. Manual QIAmp extraction method with enzyme pre-treatment resulted the most sensitive for detection of bacterial load. Sensitivity of this novel assay ranged between 10 and 103 CFU per PCR reaction forE. coliandS. aureusin human whole blood samples depending on the extraction methods used. Analysis of plasma samples showed a 10- to 100-fold reduction of bacterial 23S rDNA in comparison to the corresponding whole blood specimens, thus indicating that whole blood is the preferential sample type to be used in this real-time PCR protocol. Our results thus show that the 23S rDNA gene represents an optimal target for bacteria quantification in human whole blood.


2020 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Nasrullah Undre ◽  
Imran Hussain ◽  
John Meijer ◽  
Johannes Stanta ◽  
Gordon Swan ◽  
...  

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