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A total of 250 µL scFv-Fc fusion protein with a final concentration of 2 µg/mL in blocking solution was incubated for 1.5 h and washed three times with PBS.
Coverslips were washed and incubated in 1X PBS pH 7.4 containing 5% FBS and 3% BSA (blocking solution) for at least 30 min. Primary antibody diluted in blocking solution was incubated for 30 60 min, the coverslips washed 3X with blocking buffer and then incubated for 30 60 min with secondary antibodies: Alexa Fluor 594 for mouse diluted 1 2000 in blocking buffer.
Primary antibody (in blocking solution) was incubated for 60 min and then washed three times with blocking solution.
An anti-Sjda monoclonal antibody (2 mg/ml) diluted 1 500 in blocking solution was incubated with the parasites at 4°C overnight.
Horseradish peroxidase-conjugated secondary antibody (1/5000 or 1/1000 [for cyclin D1] dilution) in blocking solution was incubated with the membrane for 1 h at 20°C.
Antibody solution (anti-Digoxigenin-AP, Fab fragments from Roche diluted 1 4000 in blocking solution) was incubated ON at 4°C, followed by 3×15 min washes in blocking solution and 3×15 min in NTMT (0.1 M Tris-HCl pH 9.5, 0.1 M NaCl, 0.05 M MgCl, 1 mM Levamisol, 0.1% Tween-20).
Similar(54)
Primaries antibodies (prediluted in blocking solution) were incubated ON at 4°C (Rabbit anti HA 1∶300, Bethyl Cat. No. A190-108A; Mouse anti Synaptopodin 1∶80, Progen Cat. No. 61094).
pY397FAK, vinculin, or pY118 paxillin antibodies (1 100 in blocking solution) were incubated overnight at 4°C.
Primary antibodies diluted in blocking solution were incubated over night at 4 °C.
Primary antibodies prepared in blocking solution were incubated overnight at 4ºC.
Different dilutions (1 10,000 to 1 2,000) of rabbit primary polyclonal antibodies (H3K9me3 antibody ab8898 lot GR102573-1, H3K4me3 antibody ab8580 lot GR56122-1) in blocking solution were incubated with the array under mild rocking at 4°C for 1 hour.
More suggestions(16)
blocking solution was composed
blocking solution was performed
blocking solution was drawn
blocking solution was washed
blocking solution was allowed
blocking solution was aspirated
blocking solution was added
blocking solution was used
blocking solution was discarded
blocking solution was followed
blocking peptide was incubated
blocking solution was drained
blocking tissue was incubated
blocking solution was replaced
blocking solution were incubated
blocking buffer was incubated
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