Sentence examples for buffer were coated into from inspiring English sources

NVP-NAC-BSA, BSA, or KLH (100 μL, 10 μg/mL in carbonate bicarbonate coating buffer) were coated into the wells of a flat-bottom 96-well plate (Costar, Cambridge, MA), and the plate was incubated overnight at 4 °C.

Briefly, fluorescent beads were coated with Omp29 in bicarbonate buffer (pH 9.6) for 2 hr at 27°C.

ELISA plates (96 wells from Nunc) were coated with recombinant SpSsp1 (5–8 μg ml−1 in coating buffer (0.05 M carbonate/bicarbonate buffer [pH 9.6]), 50 μl per well) and left to incubate overnight at 4 °C.

Ninety six-well microtiter plates (Nunc, Maxisorpt Glostrup, Denmark) were coated with 0.5 μg of GFP protein in coating buffer, ie: 0.1 M bicarbonate buffer pH 9.6, overnight at 4°C.

The plates were coated with 100  μL of ES antigen in coating buffer (0.05 M carbonate bicarbonate-buffer, pH 9.6) and incubated at 4°C overnight.

The results indicated that the electroosmotic flow (EOF) in channels that were coated with the polymer could be reversed in 1× TBE buffer or 1× SSC buffer.

Individual wells of polystyrene 96-well flat bottom plates (NUNC) were coated with 1 μg/ml of K19M peptide diluted in coating buffer (0.05 M carbonate buffer pH 9.6) by incubation overnight at 4°C.

ELISA plates were coated with 100 μl/well of 5 μg/ml RgpB or coating buffer alone (50 mM carbonate buffer, pH 9.5), and incubated overnight at 4 °C.

Enzyme-linked immunosorbent assay (ELISA) plates (96-well, flat-bottomed, NUNC) were coated overnight at 4°C with mBSA (10 μg/ml) diluted in coating buffer (50 m M bicarbonate/carbonate buffer).

96-well Polysorp microtiter plates (Nunc) were coated overnight with UV-inactivated WSN-GP33/66 WSN-GP33/66e buffer.

Ninety-six wELISALISA microtiter plates (Corning Incorporated, USA) were coated at 1  μg/mL hE16 mAb in coating buffer (100 mM Na2CO3, pH 9.6) overnight at 4°C.