Exact(1)
Whole cell extracts dissolved in a buffer (50 mM Tris-HCl pH 6.8, 2% SDS, 10% glycerol, 100 mM dithiothreitol) or the subcellular fractions described below were separated by SDS/7.5 15% polyacrylamide gel electrophoresis, and transferred to a nitrocellulose membrane.
Similar(59)
Each frame in the composite animations below is separated by 15 minutes.
Two subgroups of the nodes below the synthetic network were separated by high or low values of eigenvector centrality.
Proteins were separated by SDS-PAGE.
Samples were boiled for 5 min and equal amounts of protein (as determined using bound Coumassie blue [below]) from each sample were separated by SDS-PAGE.
Supernatant and cells were separated by centrifugation.
Three injections were separated by 24 hours.
Individual trials were separated by 4 s.
Monocytes were separated by two different methods.
The runs were separated by short breaks.
Briefly, the individual saliva proteins were separated by 2-D SDS-PAGE and the gel was stained with silver, as described below.
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