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Part 2. Electrophoretic mobility of mixed protein + surfactant systems.
There are several theories of the dynamic electrophoretic mobility.
There are several theories that link electrophoretic mobility with zeta potential.
It is similar to electrophoretic mobility, but at high frequency, on a scale of megahertz.
Electrophoretic mobility is low and this requires high electric field, by factor 10 and higher.
Electrophoretic mobility shift assays were performed essentially as previously described (34).
This method is used for measuring electrophoretic mobility and then calculating zeta potential.
"A theoretical and experimental study of the effect of protein concentration on the electrophoretic mobility"
The Doppler shift is proportional to the electrophoretic mobility of a macromolecule.
NS5A has two phosphorylated forms: p56 and p58, which differ in the electrophoretic mobility.
The 968-1401 fragment amplified from all Arthrobacter strains had a similar electrophoretic mobility.
One group included seven esterase bands which showed constant electrophoretic mobilities at different growth temperatures.
Intermediates were tentatively identified as to chain composition from their electrophoretic mobilities.
An electrophoretic mobility curve method was found useful in the interpretation of the enzyme spectra.
The electrophoretic mobility can be determined experimentally from the migration time and the field strength:
Samples were then subjected to an electrophoretic mobility shift assay as described previously (24).
Immunofixation identifies antibodies in a mixture as a function of their specific electrophoretic mobility.
Thus, the electrophoretic mobility depends not only on the charge-to-mass ratio, but also to the physical shape and size of the protein.
Anionic dyes of a known electrophoretic mobility are usually included in the sample buffer.
The electrophoretic mobility of prolactin varied diurnally and with change in photoperiod.
The electrophoretic mobility of both asialotransferrins increased with time, type 2 being affected sooner than type 1.
These different rates of advancement (different electrophoretic mobilities) separate into bands within each lane.
An electrophoretic mobility shift assay can assess whether a structure incorporates all desired strands.
Binding of cationic particles and measurement of cellular electrophoretic mobility.
Figure 3 indicates that complexes exhibiting the same electrophoretic mobility were generated with all three extracts.