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Exact(8)
Proteins were eluted in Laemmli sample buffer and were analyzed by SDS-PAGE followed by immunoblot with indicated antibodies.
Cells were washed twice in Staining Buffer and were analyzed using LSR 1 or LSRII (BD Bioscience) in the Stanford Shared FACS Facility.
The lysates were prepared from dissected sensory epithelia using hypotonic buffer and were analyzed by Western blotting either before or after endoglycosidaseF treatment (Roche, Indianapolis, IN).
Samples were washed in BSA buffer and were analyzed on a FACS Calibur.
After washing cells were resuspended in 400 μl of FACS buffer and were analyzed using a LSRII FACS machine (BD Bioscience, Heidelberg, Germany).
Following rigorous washing steps, samples were resuspended in 0.5 ml of FACS buffer and were analyzed using a LSRII FACS machine (BD Bioscience, Heidelberg, Germany).
Similar(52)
The cells were washed in PhosFlow Perm/Wash Buffer I, and were analyzed by flow cytometry, as already described.
The reaction was stopped by adding the SDS-PAGE loading buffer and was analyzed by western blot and autoradiography.
The total lysis was mixed with an equal volume of 2× SDS sample buffer and was analyzed by Western blotting.
The representative samples (5.0 g each) were extracted using the acetate buffered extraction under the optimized conditions and were analyzed using HPLC system of the reported methods.
Bead-coupled proteins were washed three times in binding buffer containing 1 M KCl and boiled in Laemmli buffer, and supernatants were analyzed by western blot analysis with α-RSK2 antibodies (Santa Cruz Biotechnology).
More suggestions(17)
buffer and were assayed
buffer and were boiled
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 fractionated
buffer and were separated
buffer and were transported
buffer and were transferred
buffer and were injected
buffer and were resuspended
buffer and were added
buffer and were frozen
buffer and were stained
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