1,990 research outputs found
PraQ-A Scale Handbook: Students' Learning Growth Evaluation of scientific experimental labs
Scale Handbook for PraQ-A Questionnaire for Laboratory quality described in Publications by Daniel Rehfeldt. For full information about the theoretical model behind the instrument and test evaluation studies ("validity"), see: Rehfeldt, D. (2018). Erfassung der Lehrqualität naturwissenschaftlicher Experimentalpraktika – Dissertationsschrift (Band 246). Berlin: Logos
The First Fifty Years of the History of the Igreja Evangelica Lutherana Do Brazil, The Brazilian District of the Missouri Synod
The present study is an attempt to describe and to analyze the main developments of the work of the Missouri Synod in Brazil during the first half of the twentieth century, from the beginning of its missionary- work in Brazil in 1900 to 1950
Sulfo-SMCC Prevents Annealing of Taxol-Stabilized Microtubules In Vitro
Microtubule structure and functions have been widely studied in vitro and in
cells. Research has shown that cysteines on tubulin play a crucial role in the
polymerization of microtubules. Here, we show that blocking sulfhydryl groups
of cysteines in taxol-stabilized polymerized microtubules with a commonly used
chemical crosslinker prevents temporal end-to-end annealing of microtubules in
vitro. This can dramatically affect the length distribution of the
microtubules. The crosslinker sulfosuccinimidyl
4-(N-maleimidomethyl)cyclohexane-1-carboxylate, sulfo-SMCC, consists of a
maleimide and an N-hydroxysuccinimide ester group to bind to sulfhydryl groups
and primary amines, respectively. Interestingly, addition of a maleimide dye
alone does not show the same interference with annealing in stabilized
microtubules. This study shows that the sulfhydryl groups of cysteines of
tubulin that are vital for the polymerization are also important for the
subsequent annealing of microtubules.Comment: 3 figure
The Filament Sensor for Near Real-Time Detection of Cytoskeletal Fiber Structures
A reliable extraction of filament data from microscopic images is of high
interest in the analysis of acto-myosin structures as early morphological
markers in mechanically guided differentiation of human mesenchymal stem cells
and the understanding of the underlying fiber arrangement processes. In this
paper, we propose the filament sensor (FS), a fast and robust processing
sequence which detects and records location, orientation, length and width for
each single filament of an image, and thus allows for the above described
analysis. The extraction of these features has previously not been possible
with existing methods. We evaluate the performance of the proposed FS in terms
of accuracy and speed in comparison to three existing methods with respect to
their limited output. Further, we provide a benchmark dataset of real cell
images along with filaments manually marked by a human expert as well as
simulated benchmark images. The FS clearly outperforms existing methods in
terms of computational runtime and filament extraction accuracy. The
implementation of the FS and the benchmark database are available as open
source.Comment: 32 pages, 21 figure
The Other Sheep Volume 40 Number 02
https://digitalcommons.olivet.edu/cotn_os/1053/thumbnail.jp
The Other Sheep Volume 42 Number 10
https://digitalcommons.olivet.edu/cotn_os/1085/thumbnail.jp
The Other Sheep Volume 41 Number 01
https://digitalcommons.olivet.edu/cotn_os/1064/thumbnail.jp
The Other Sheep Volume 37 Number 12
https://digitalcommons.olivet.edu/cotn_os/1011/thumbnail.jp
The Other Sheep Volume 39 Number 05
https://digitalcommons.olivet.edu/cotn_os/1044/thumbnail.jp
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