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Exact(6)
The bound proteins were eluted with SDS loading buffer and were separated by SDS/PAGE followed by immunoblotting with antibody against STAT3 (Santa Cruz Biotechnology, Dallas, TX, USA).
Cell lysates were boiled in Laemmli sample buffer and were separated by SDS-PAGE, transferred to nitrocellulose filters, probed with the antibody of interest, and developed using ECL (Amersham Biosciences, Pittsburg, PA, USA).
Then, samples were reduced with β-mercaptoethanol in Laemmli sample buffer and were separated by SDS-PAGE electrophoresis.
Proteins bound to the beads were eluted with 2 × SDS-PAGE sample buffer and were separated on an SDS-PAGE gel.
The samples of surnatants were thereafter diluted with reducing sample buffer and were separated by electrophoresis on a 10% SDS-PAGE gel (20 μg protein per lane loaded).
The retained peptides were washed with the same buffer and were separated on a PicoFrit Analytical Columns (ProteoPep II C18, 300 Å, 5 μm, 50 μm × 100 mm, tip ID=10 μm, New Objective, Inc).
Similar(54)
Eluates were vacuum dried and resuspended in protein sample buffer (1×MES buffer+1×protein loading buffer, Life Technologies) and were separated by SDS-PAGE on a 10 20% NuPAGE gradient gel (Life Technologies).
A total of 20 μg protein was boiled in the presence of 6 × sodium dodecyl sulfate sample buffer, and was separated on 7.5% or 10% sodium dodecyl sulfate-polyacrylamide gel (ATTO, Tokyo, Japan).
Briefly, human ADSC samples and epithelial-like cells were selected using the same method, lysed in RIPA buffer and protein lysates and were separated on 8 % SDS polyacryamide gel by electrophoresis.
The beads were washed three times with lysis buffer, and immunoprecipitates were separated from the beads by adding 2× sample buffer and boiled and fractioned by SDS PAGE.
The beads were washed three times with lysis buffer and immunoprecipitates were separated from the beads by adding 2× sample buffer and boiled.
More suggestions(15)
buffer and were studied
buffer and were used
buffer and were heated
buffer and were bubbled
buffer and were lysed
buffer and were subjected
buffer and were transported
buffer and were transferred
buffer and were injected
buffer and were resuspended
buffer and were analyzed
buffer and were added
buffer and were frozen
buffer and were stained
buffer and were analysed
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