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Excess acid was removed with ethanol.
Deposited drugs in the device, throat, and cups were removed with ethanol and collected in volumetric flasks.
Unbound ThS was removed with ethanol (50%%, 2×1 min) and distilled water (1×5 min).
Similar(57)
The staining reaction was stopped by adding distilled water, the color of chlorophyll was removed with 70% ethanol (v/v) several times, and seedlings were soaked in 95% ethanol (v/v) for 1 h.
After staining, chlorophyll in the tissue was removed with 95% ethanol.
Thin paraffin sections were deparaffinized with xylene, and the xylene was removed with 100% ethanol.
The sections were deparaffinised in xylene, and xylene was subsequently removed with absolute ethanol.
Residual xylene was removed with 100% ethanol and the tubes were allowed to stand for 10 min at room temperature.
Leaf chlorophylls were removed with 95% ethanol before visualizing under a light microscope as described by Ishiga et al. [ 53].
The ethanol was removed with isoamyl acetate-ethanol solution (1 1, v:v), incubated for 10 min, and centrifuged at 12,000 rpm for 5 min.
Excess PTAD was removed with 400 μL ethanol and the supernatant was then again dried under a stream of nitrogen.
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