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Exact(21)
Both the dsRNA of GFP and an equivalent volume of buffer were used as controls.
Plant incubated with 20 ml of wash buffer were used as a control.
To detect the EPS shed from M. xanthus cells onto different surfaces, 50 µl DK1622 or SW504 cells at 1×108 cell/ml in MOPS buffer was added to the wells of Costar™ polystyrene 96-well plates w/wo SuperBlock pre-treatment while 50 µl of MOPS buffer and 50 µl purified EPS (10 µg/ml carbohydrate in MOPS buffer) were used as controls.
Paclitaxel and general tubulin buffer were used as controls.
Serum-free and medium-containing FBS or lysis buffer were used as background controls.
A group of 3 mice injected with PBS buffer were used as uninfected control.
Similar(39)
Acetate buffer was used as the blank.
PBS buffer was used as a negative control.
The TB medium without glycerol and PBS buffer was used as the control.
Hence, 30 mM phosphate buffer was used as the aqueous phase in this study.
0.1 M phosphate buffer was used as it gaves the highest number of theoretical plates with good resolution.
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