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Exact(20)
The supernatant was allowed to bind to the column overnight at 4 °C.
Briefly, rabbit antisera were diluted 1∶2 and passed through protein G columns enabling antibodies to bind to the column.
Protein that did not bind to the column was kept for analysis of the inner core of the LB.
Thus, this protein cannot bind to the column, probably due to degradation of the affinity tag.
C1q does not bind to the column, but contaminants were removed.
At pH 8.0, the Nf xylF did not bind to the column.
Similar(40)
When we characterized the binding of the complement regulators C1INH, C4BP, and factor H by Western blotting (Fig. 1B), we found that in the presence of C1q, C1INH, factor H and C4BP bound to the column, but after C1q depletion, binding of C1INH was no longer seen, suggesting that the protein bound to CS-A in association with C1q.
M, protein marker; hLF, human lactoferrin standard; TG, milk samples from transgenic cows; P1 and P2, rhLF eluted from the column; FT, protein fraction that was not bound to the column.
SCARB2 bound to the column was eluted in a buffer containing 50 mmol/L imidazole.
Proteins bound to the column were then eluted with elution buffer (column buffer with 1 M NaCl).
MtbHadAB complex bound to the column was eluted with a 0.05 1 mol/L linear gradient of NaCl.
More suggestions(16)
bind to the surface
bind to the novel
bind to the peptide
bind to the promoter
bind to the tyrosinase
bind to the target
bind to the active-site
bind to the basal
bind to the AhR
bind to the recognition
bind to the lipophilic
bind to the enzyme
bind to the interspace
bind to the sulfhydryl
bind to the duplex
bind to the estrogen
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