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Exact(11)
After incubation at 4°C overnight with gentle shaking, the resin was extensively washed with the wash buffer and then eluted with the elution buffer (20 mM Tris-HCl, pH 7.8, 400 mM NaCl, 300 mM imidazole and 0.2% DPC).
The column was washed with 5 bed-volume of amylose resin wash buffer and then eluted with 10 bed-volume of amylose resin elution buffer (20 mM maltose in amylose resin wash buffer) followed by 0.5 M NaOH wash of the column.
The precipitated beads were washed at least four times with the protein extraction buffer and then eluted by 2 × SDS protein-loading buffer with boiling for 5 min.
The sample was rinsed with the same buffer and then eluted with the same buffer containing 0.01 M NaCl at a flow rate of 20 ml/h.
The column was rinsed thoroughly with the same buffer and then eluted with 100 mM methyl-α-d-mannoside in the buffer at a flow rate of 20 ml/h.
The column was washed with 4 ml of the same buffer and then eluted using a 20 mL gradient of NaCl (0 0.5 M) at a flow rate of 0.5 ml/min.
Similar(49)
DNA (35 μg) was bound to the CXXC matrix in a 100 mM NaCl-containing column buffer, washed and then eluted using buffer containing 1 M NaCl.
The F3 sample, which included Cel7A and Bgl3A, was applied to a Source 15S cation-exchange column equilibrated with buffer B and then eluted with the same buffer.
Digests were loaded in 2% acetonitrile/0.1% formic acid (Buffer A) and then eluted with a linear gradient of buffer B (100%acetonitrile/0.1%% formic acid) at 300 nL/min.
The columns were washed with 8 ml of 10 and 20 mM imidazole in buffer A and then eluted step-wise with 2.5 ml aliquots of buffer A containing 50, 100, 250, and 500 mM imidazole.
After the cation exchange column was removed away, the protein was washed with 40 ml buffer A, and then eluted using a 0 1.0 M NaCl gradient in the same buffer with a speed of 1 ml/min.
More suggestions(15)
buffer and then centrifuged
buffer and then dried
buffer and then transmitted
buffer and then used
buffer and then retransmitted
buffer and then processed
buffer and then derivatized
buffer and then immunoblotted
buffer and then examined
buffer and then suspended
buffer and then diluted
buffer and then pooled
buffer and then overlaid
buffer and then added
buffer and then denatured
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