Facile Green In Situ Synthesis of Mg/CuO Core/Shell Nanoenergetic Arrays with a Superior Heat-Release Property and Long-Term Storage Stability

2013 ◽  
Vol 5 (15) ◽  
pp. 7641-7646 ◽  
Author(s):  
Xiang Zhou ◽  
Daguo Xu ◽  
Qiaobao Zhang ◽  
Jian Lu ◽  
Kaili Zhang
2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Ying Zhu ◽  
Xiang Zhou ◽  
Chun Wu ◽  
Hua Cheng ◽  
Zhouguang Lu ◽  
...  

2019 ◽  
Vol 55 (18) ◽  
pp. 2660-2663 ◽  
Author(s):  
Yucheng Liu ◽  
Guobin Mao ◽  
Wang Wang ◽  
Songbai Tian ◽  
Xinghu Ji ◽  
...  

In this work, the electron transfer protein cytochrome c is innovatively embedded into cellulose paper to prepare photoluminescence-quenching nanopaper with a highly-efficient quenching ability, rapid reaction time and long-term storage.


ACS Omega ◽  
2020 ◽  
Vol 5 (42) ◽  
pp. 27171-27179 ◽  
Author(s):  
Indika K. Warnakula ◽  
Afshin Ebrahimpour ◽  
Sun Yi Li ◽  
Ramesha D. Gaspe Ralalage ◽  
Chathuranga C. Hewa-Rahinduwage ◽  
...  

2011 ◽  
Vol 59 (12) ◽  
pp. 1113-1121 ◽  
Author(s):  
Christina Karlsson ◽  
Mats G. Karlsson

Storage of tissue slides has been claimed to induce dramatically reduced antigen detection particularly for immunohistochemistry (IHC). With tissue microarrays, the necessity to serially cut blocks in order to obtain as much material as possible is obvious. The presumed adverse effect of storage might hamper such an approach. The authors designed an experimental setting consisting of four different storage conditions with storage time of tissue slides of up to 1 year. Detection of proteins, DNA, and mRNA was performed using IHC and in situ hybridization techniques. Slight but significant changes in IHC occurred over time. The most important factor is the primary antibody used: four showed no significant changes, whereas limited decreases in 8 antibodies could be detected by image analysis. Whether the antigen was nuclear or cytoplasmic/membranous did not matter. No major differences between different storage conditions could be shown, but storage at 4C was overall the best procedure. Furthermore, gene copy number aberrations, chromosomal translocations, and the presence of mRNA could be detected on slides stored up to 1 year. In conclusion, in tissues optimally formalin fixed and using modern histological techniques, only minute changes in tissue antigenicity are induced by long-term storage.


2004 ◽  
Vol 93 (10) ◽  
pp. 2609-2623 ◽  
Author(s):  
Derrick S. Katayama ◽  
Carol F. Kirchhoff ◽  
Carrie M. Elliott ◽  
Robert E. Johnson ◽  
Jeffry Borgmeyer ◽  
...  

2018 ◽  
Vol 1 (5) ◽  
pp. 2184-2194 ◽  
Author(s):  
Jie Feng ◽  
Yingyue Zhang ◽  
Simon A. McManus ◽  
Kurt D. Ristroph ◽  
Hoang D. Lu ◽  
...  

Energy ◽  
2019 ◽  
Vol 186 ◽  
pp. 115882 ◽  
Author(s):  
Wenfei Cai ◽  
Ning Kang ◽  
Moon Ki Jang ◽  
Chen Sun ◽  
Ronghou Liu ◽  
...  

1996 ◽  
Vol 59 (5) ◽  
pp. 481-486 ◽  
Author(s):  
HSING-YI HSIEH ◽  
BONITA A. GLATZ

Propionicin PLG-1, a bacteriocin produced by Propionibacterium thoenii strain P127, was tested for characteristics that could determine its usefulness as a food preservative: long-term storage stability and effectiveness in a food model system. Partially purified propionicin PLG-1 samples, lyophilized and nonlyophilized, were stored at 25, 4, and −20°C. Bacteriocin activity increased by as much as 200% over the first 10 days of storage in nonlyophilized samples stored at 25 or 4°C. Activity then decreased gradually for samples stored at 25°C while samples stored at 4°C retained high activity through 14 weeks of storage. Nonlyophilized samples frozen at −20°C and lyophilized samples stored at all temperatures did not change significantly in activity through 25 weeks of storage. Propionicin was added at 100 and 1,000 arbitrary units (AU)/ml to lactobacilli MRS broth and to skim milk, each inoculated with 105 cells per ml of Lactobacillus delbrueckii ATCC 4797. Upon incubation at 37°C with 1,000 AU/ml, cell numbers were reduced by at least 4 log units within 2 h and no viable cells were detected after 96 h in either medium. With 100 AU/ml of propionicin, viable cells were reduced by 2 log units within 12 h at 37°C, but culture growth resumed after 24 h. At 15°C, no viable cells were detected after 48 h in the presence of 1,000 AU/ml of propionicin, while viable cell counts were gradually reduced to about 10 cells per ml by 168 h in the presence of 100 AU/ml of propionicin.


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