Results 21 to 30 of about 1,322,177 (348)

Histo-pathology study of the growth of Trichoderma harzianum, Phaeomoniella chlamydospora and Eutypa lata on grapevine pruning wounds

Phytopathologia Mediterranea, 2011
Protecting grapevine pruning wounds by inoculating them with Trichoderma spp. can preventinfection from trunk disease pathogens. The growth and interactions of both, the biological control agent Trichoderma spp.
Cheusi MUTAWILA, Paul FOURIE, Francois HALLEEN, Lizel MOSTERT   +3 more
doaj   +1 more source

Fluorescent Protein Approaches in Alpha Herpesvirus Research

Viruses, 2015
In the nearly two decades since the popularization of green fluorescent protein (GFP), fluorescent protein-based methodologies have revolutionized molecular and cell biology, allowing us to literally see biological processes as never before.
Ian B. Hogue, Jens B. Bosse, Esteban A. Engel, Julian Scherer, Jiun-Ruey Hu, Tony del Rio, Lynn W. Enquist   +6 more
doaj   +1 more source

Improved split fluorescent proteins for endogenous protein labeling. [PDF]

, 2017
Self-complementing split fluorescent proteins (FPs) have been widely used for protein labeling, visualization of subcellular protein localization, and detection of cell-cell contact.
Feng, Siyu, Huang, Bo, Leonetti, Manuel D, Li, Han, Pessino, Veronica, Sekine, Sayaka   +5 more
core   +2 more sources

Fluorescent Protein-Based Metal Biosensors

Chemosensors, 2023
Fluorescent proteins (FPs) are optical probes that are used to track the functions of genetically encoded target molecules in molecular and cellular biology.
Ki Hyun Nam
doaj   +1 more source

Translational and rotational motions of albumin sensed by a non-covalent associated porphyrin under physiological and acidic conditions: a fluorescence correlation spectroscopy and time resolved anisotropy study. [PDF]

, 2008
The interaction between a free-base, anionic water-soluble porphyrin, TSPP, and the drug carrier protein, bovine serum albumin (BSA) has been studied by time-resolved fluorescence anisotropy (TRFA) and fluorescence correlation spectroscopy (FCS) at two ...
Andrade, S.M., Borst, J.W., Costa, S.M., Hoek, A., van, Visser, A.J.W.G.   +4 more
core   +2 more sources

Nuclear Import Analysis of Two Different Fluorescent Marker Proteins into Hepatocyte Cell Lines (HuH-7 Cell)

Indonesian Journal of Biotechnology, 2005
The application of fluorescent proteins as expression markers and protein fusion partners has proved immensely valuable for resolving the organization of biological events in living cells.
Aris Haryanto, Michael Kann
doaj   +1 more source

Ratiometric Matryoshka biosensors from a nested cassette of green- and orange-emitting fluorescent proteins

Nature Communications, 2017
Single fluorescent protein biosensors are susceptible to expression and instrumental artifacts. Here Ast et al. describe a dual fluorescent protein design whereby a reference fluorescent protein is nested within a reporter fluorescent protein to control ...
Cindy Ast, Jessica Foret, Luke M. Oltrogge, Roberto De Michele, Thomas J. Kleist, Cheng-Hsun Ho, Wolf B. Frommer   +6 more
doaj   +1 more source

Homotransfer FRET Reporters for Live Cell Imaging

Biosensors, 2018
Förster resonance energy transfer (FRET) between fluorophores of the same species was recognized in the early to mid-1900s, well before modern heterotransfer applications.
Nicole E. Snell, Vishnu P. Rao, Kendra M. Seckinger, Junyi Liang, Jenna Leser, Allison E. Mancini, M. A. Rizzo   +6 more
doaj   +1 more source

Electrochemical fluorescence switching of enhanced green fluorescent protein

Biosensors and Bioelectronics, 2023
Switchable fluorescent proteins, for which fluorescence can be switched ON and OFF, are widely used for molecule tracking and super resolution imaging. However, the robust use of the switchable fluorescent proteins is still limited as either the switching is not repeatable, or such switching requires irradiation with coupled lasers of different ...
Yang, Y, Fan, S, Webb, JA, Ma, Y, Goyette, J, Chen, X, Gaus, K, Tilley, RD, Gooding, JJ   +8 more
openaire   +3 more sources

Controlled assembly of SNAP-PNA-fluorophore systems on DNA templates to produce fluorescence resonance energy transfer [PDF]

, 2014
The SNAP protein is a widely used self-labeling tag that can be used for tracking protein localization and trafficking in living systems. A model system providing controlled alignment of SNAP-tag units can provide a new way to study clustering of fusion ...
Bader A. N., Bannwarth M., Brun M. A., Campos C., Carrion-Vazquez M., Chakrabarti R., Dadon Z., Daguer J. P., Diaz-Mochon J. J., Donovan C., Feldkamp U., Gautier I., Gholami Z., Gorska K., Gronemeyer T., Harris J. L., Haruki H., Hermanson G. T., Hinner M. J., Huang K.-T., Hussain A. F., Hutchins B. M., Johnsson K., Johnsson N., Juillerat A., Jung D., Kamiya M., Kampmeier F., Kazane S. A., Keppler A., Keppler A., Keppler A., Keppler A., Komatsu T., Lakowicz J. R., Lin M. Z., Lo P. K., Lovrinovic M., Lu H., Maurel D., Menchise V., Niemeyer C. M., Niemeyer C. M., Niemeyer C. M., O’Hare H. M., Pianowski Z. L., Pin J. P., Pouchain D., Prencipe G., Quentin Hanley, Roloff A., Rothemund P. W. K., Rothlingshofer M., Rozners E., Runnels L. W., Sadhu K. K., Scheibe C., Scheibe C., Scheibe C., Seeman N. C., Spinelli N., Sun X., Svensen N., Urbina H. D., Weber G., Weber G., Winssinger N., Yeow E. K. L., Zahra Gholami, Zolmajd-Haghighi Z.   +69 more
core   +1 more source