Faculty Opinions recommendation of Reducing background fluorescence reveals adhesions in 3D matrices.

Author(s):  
Christopher Chen ◽  
Daniel Cohen
1979 ◽  
Vol 27 (1) ◽  
pp. 96-101 ◽  
Author(s):  
T Hirschfeld

A number of electrooptical techniques are described that discriminate against background fluorescence in biologic staining, whether from sample background or unbound excess stain. These techniques are based on the fluorescent decay lifetime difference between bound stain and the sample background or between the bound stain its free form. The fluorescence decay lifetimes may be measured either directly or in a combination gated photometry scheme to substantially enhance the sample background contrast. An alternative procedure uses the photochemical bleaching of fluorescent dyes under intense exposure to time discriminate with higher selectivity, sensitivity and in a more convenient fashion between diverse fluorescent molecules.


2017 ◽  
Vol 15 (02) ◽  
pp. 1650041 ◽  
Author(s):  
M. Sh. Barkovskaya ◽  
A. G. Bogomolov ◽  
N. Yu. Knauer ◽  
N. B. Rubtsov ◽  
V. A. Kozlov

Telomere length is an important indicator of proliferative cell history and potential. Decreasing telomere length in the cells of an immune system can indicate immune aging in immune-mediated and chronic inflammatory diseases. Quantitative fluorescent in situ hybridization (Q-FISH) of a labeled (C3TA[Formula: see text] peptide nucleic acid probe onto fixed metaphase cells followed by digital image microscopy allows the evaluation of telomere length in the arms of individual chromosomes. Computer-assisted analysis of microscopic images can provide quantitative information on the number of telomeric repeats in individual telomeres. We developed new software to estimate telomere length. The MeTeLen software contains new options that can be used to solve some Q-FISH and microscopy problems, including correction of irregular light effects and elimination of background fluorescence. The identification and description of chromosomes and chromosome regions are essential to the Q-FISH technique. To improve the quality of cytogenetic analysis after Q-FISH, we optimized the temperature and time of DNA-denaturation to get better DAPI-banding of metaphase chromosomes. MeTeLen was tested by comparing telomere length estimations for sister chromatids, background fluorescence estimations, and correction of nonuniform light effects. The application of the developed software for analysis of telomere length in patients with rheumatoid arthritis was demonstrated.


The Analyst ◽  
2016 ◽  
Vol 141 (20) ◽  
pp. 5784-5791 ◽  
Author(s):  
Qiang Su ◽  
Gilbert Nöll

Cutting surface-bound optical molecular beacons results in a sandwich-like detection strategy with lower background fluorescence.


2017 ◽  
Vol 28 (10) ◽  
pp. 1987-1990 ◽  
Author(s):  
Dan Cheng ◽  
Yue Pan ◽  
Bin-Cheng Yin ◽  
Lin Yuan ◽  
Xiao-Bing Zhang

2014 ◽  
Author(s):  
F. Fantoni ◽  
L. Hervé ◽  
V. Poher ◽  
S. Gioux ◽  
J. I. Mars ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Xiaoxia Wu ◽  
Xiaofeng Tian ◽  
Lihua Xu ◽  
Jiutong Li ◽  
Xinxia Li ◽  
...  

Harsh demanding has been exposed on the concentration of aflatoxin M1 (AFM1) and chloramphenicol (CAP) in milk. In this study, we developed a new method based on background fluorescence quenching immunochromatographic assay (bFQICA) to detect AFM1 and CAP in milk. The detection limit for AFM1 was 0.0009 ng/mL, while that for the CAP was 0.0008 ng/mL. The assay variability was determined with 3 AFM1 standards (i.e., 0.25 ng/mL, 0.5 ng/mL, and 1.0 ng/mL), and the actual detection value was 0.2497, 0.5329, and 1.0941, respectively. For the assay variability of 3 CAP standards (i.e., 0.10 ng/mL, 0.30 ng/mL, and 0.50 ng/mL), the actual detection value was 0.0996, 0.3096, and 0.4905, respectively. The recovery rate of AFM1 was 99.7%–101.7%, while that for CAP was 95.3%–97.6%. For the test stability, AFM1 and CAP showed satisfactory test stability even at month 5. Compared with the sensitivity of liquid chromatography-mass spectrometry (LC-MS) method, no statistical difference was noticed in results of the bFQICA. Our method is convenient for the detection of AFM1 and CAP in milk with a test duration of about 8 minutes. Additionally, an internal WiFi facility is provided in the system allowing for quick connection and storage in the intelligent cell phone.


2005 ◽  
Vol 04 (04) ◽  
pp. 695-700 ◽  
Author(s):  
U. S. DINISH ◽  
Z. X. CHAO ◽  
L. K. SEAH ◽  
V. M. MURUKESHAN

The extension of fluorescence measurements of samples from steady state to dynamic methods offers the possibility to extract valuable information at the micro and nano level. Imaging of fluorescent samples with nanosecond resolution often imposes challenging problems, especially when dealing with very weak optical and electrical signals. In this context, this paper discusses the detection of latent fingerprint samples with nanosecond resolution. Imaging of fingerprint samples, which are deposited on strongly fluorescing substrates, is carried out by the subsequent suppression of the unwanted background fluorescence emissions using the time-resolved optical technique. "signature" characterisation of fingerprint samples treated with fluorescent magnetic powders is also carried out.


2013 ◽  
Vol 33 (2) ◽  
pp. 0230002 ◽  
Author(s):  
高国明 Gao Guoming ◽  
李雪 Li Xue ◽  
覃宗定 Qin Zongding ◽  
魏坤莲 Wei Kunlian ◽  
黄汉明 Huang Hanming ◽  
...  

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