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Exact(23)
Reactions were stopped by mixing with SDS-PAGE loading buffer and resolved on SDS-PAGE gels.
Forty micrograms of protein were mixed with sample buffer and resolved on 10% SDS-PAGE.
For immunoblot analysis, 30 µg of protein was boiled in Laemmli buffer and resolved on 10% gel.
The proteins were extracted from enriched parasites by boiling in SDS sample buffer and resolved on an SDS PAGE gel.
Then, 50 µg of protein were heat denatured in SDS-PAGE sample buffer and resolved on denaturing (SDS) 10% polyacrylamide gels (SDS-PAGE).
The cytosolic and nuclear fractions were boiled in 2× Laemmli sample buffer and resolved on a 10% SDS polyacrylamide gel and probed with a phospho Erk1/2 antibody.
Similar(37)
Reactions are divided into two equal aliquots and diluted two fold with SDS-PAGE, or native-PAGE gel loading buffers, and resolved on SDS or native gels, followed by autoradiography.
The GST beads were washed three times with GST-buffer and resolved on SDS PAGE followed by Coomassie dye staining.
Finally, the bound material was eluted from the beads using 80°C 1× SDS loading buffer (Invitrogen) and resolved on 4 12% PAGE (NuPage, Invitrogen), followed by protein band detection with Coomassie Blue R (Sigma) staining.
The eluted scFv was dialyzed against 50 mM Tris-NaCl buffer overnight and resolved on a 15 % SDS-PAGE for the analysis of its purity.
The precipitate was solubilized in SDS sample buffer (Bio-Rad) and resolved on 10% or 4 20% Tris-HCl Rgels (Bio-Rad).
More suggestions(16)
buffer and analyzed on
buffer and visualized on
buffer and stirred on
buffer and kept on
buffer and layered on
buffer and placed on
buffer and separated on
buffer and sonicated on
buffer and homogenized on
buffer and depended on
buffer and fractionated on
buffer and incubated on
buffer and chilled on
buffer and mounted on
buffer and applied on
buffer and lysed on
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