scholarly journals Combination of On-Chip Field Amplification and Bovine Serum Albumin Sweeping for Ultrasensitive Detection of Green Fluorescent Protein

2009 ◽  
Vol 81 (13) ◽  
pp. 5333-5341 ◽  
Author(s):  
Qiong Pan ◽  
Meiping Zhao ◽  
Shaorong Liu
Keyword(s):  
Green Fluorescent Protein ◽  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Fluorescent Protein ◽  
Ultrasensitive Detection ◽  
Field Amplification ◽  
On Chip ◽  
Green Fluorescent

Ultrasensitive detection of nonlabelled bovine serum albumin using photothermal optical phase shift detection with UV excitation

The Analyst ◽  
2020 ◽  
Vol 145 (7) ◽  
pp. 2580-2585 ◽  
Author(s):  
Hisashi Shimizu ◽  
Shigenori Takeda ◽  
Kazuma Mawatari ◽  
Takehiko Kitamori
Keyword(s):  
Phase Shift ◽  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Detection System ◽  
Ultrasensitive Detection ◽  
Optical Phase ◽  
System P ◽  
Shift Detection ◽  
Uv Excitation

Ultrasensitive detection of nonlabelled bovine serum albumin is performed in micro/nanofluidic chips using a photothermal optical phase shift (POPS) detection system.

Ethyl violet–bovine serum albumin fluorescent protein nanovessels target to lysosomes and mitochondria

Nanomedicine ◽  
2019 ◽  
Vol 14 (1) ◽  
pp. 19-31
Author(s):  
Yang Liu ◽  
Yuanyuan Li ◽  
Jia Li ◽  
Zhigang Xie ◽  
Youjun Wang ◽  
...  
Keyword(s):  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Fluorescent Protein ◽  
Ethyl Violet

Rapid and ultrasensitive detection of active thrombin based on the Vmh2 hydrophobin fused to a Green Fluorescent Protein

2017 ◽  
Vol 87 ◽  
pp. 816-822 ◽  
Author(s):  
Alessandra Piscitelli ◽  
Anna Pennacchio ◽  
Paola Cicatiello ◽  
Jane Politi ◽  
Luca De Stefano ◽  
...  
Keyword(s):  
Green Fluorescent Protein ◽  
Fluorescent Protein ◽  
Ultrasensitive Detection ◽  
Green Fluorescent

d-Penicillamine and bovine serum albumin co-stabilized copper nanoclusters with remarkably enhanced fluorescence intensity and photostability for ultrasensitive detection of Ag+

2016 ◽  
Vol 40 (1) ◽  
pp. 732-739 ◽  
Author(s):  
Li Ruiyi ◽  
Wang Huiying ◽  
Zhou Xiaoyan ◽  
Liao Xiaoqing ◽  
Sun Xiulan ◽  
...  
Keyword(s):  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Fluorescence Intensity ◽  
Bovine Serum ◽  
Silver Ion ◽  
Ultrasensitive Detection ◽  
Enhanced Fluorescence ◽  
Copper Nanoclusters ◽  
High Fluorescence Intensity ◽  
High Fluorescence

This study reports the synthesis of d-penicillamine and bovine serum albumin co-stabilized copper nanoclusters. The nanoclusters show high fluorescence intensity, stability and response towards silver ion.

scholarly journals A simple fluorescent method for simultaneous determination of aortic permeability to horseradish peroxidase and bovine serum albumin.

1981 ◽  
Vol 29 (12) ◽  
pp. 1405-1410 ◽  
Author(s):  
T M Hollis ◽  
M E Katora ◽  
J Montini
Keyword(s):  
Bovine Serum Albumin ◽  
Horseradish Peroxidase ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Fluorescent Protein ◽  
Fluorescein Isothiocyanate ◽  
Mean Values ◽  
Protein Tracers ◽  
Net Uptake ◽  
Male Wistar Rats

Differences in regional aortic net uptake of bovine serum albumin (BSA) and horseradish peroxidase (HP) have been examined by means of conjugation of these molecules to the fluorescent protein tracers fluorescein isothiocyanate (FITC) and lissamine rhodamine B (RB200). Using male Wistar rats, uptake of FITC-BSA under steady state conditions in the ascending aorta and aortic arch (14 +/- 2 micrograms/mg aorta) is significantly higher (p less than 0.05) than that of either the upper, middle, or lower third of the thoracic aorta (10 +/- 1 mu, 9 +/- 1 mu, and 8 +/- 1 micrograms/mg, respectively). No regional variation in net uptake of RB200-HP was observed in these same aortic regions, with respective mean values (+/- SE) being 69 +/- 2, 69 +/- 2, 68 +/- 4, and 68 +/- 4 micrograms/mg. Examination of fluorescence photomicrographs indicate that FITC-BSA is localized along the collagen-elastin bands, while the RB200-HP is found between these bands. Differences between FITC-BSA and RB200-HP uptake and deposition reflect such things as differences in uptake rates as influenced by initial concentrations, permeability coefficients, as well as possible differences in molecular charge and affinity. The results indicate that the fluorometric procedures described in this investigation are simple, sensitive, and quantitative, and suitable for simultaneous measurement of aortic uptake of molecules having different molecular sizes as well as for the intraaortic localization of these substances.

Sign in / Sign up

Export Citation Format

Share Document