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All dried material was chopped into small fragments.
The material was chopped in a laboratory hammer mill to a particle size smaller than 3 mm.
The collected plant material was chopped into small pieces and air-dried under shade without exposing it to direct sunlight and the dried plant material was grounded to 0.5 μm sizes.
The leaf material was chopped together with the internal standard, = tetraploid Lepisorus clathratus s.l., in 0.5 ml ice-cold general-purpose buffer with the addition of 3%PVP-40PVP-40[49]
Hereby, fresh leaf material was chopped with a sharp razor blade in 100 μl of Galbraith's buffer, diluted to total volume of 1.5 ml (with Galbraith's buffer) after which the resulting nuclei suspension was filtered through a 40 μm nylon mesh.
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Raw materials were chopped manually and air dried in a greenhouse.
Through Shrobe's practice, however, the domestic materials are chopped up, rearranged and reincarnated, forming an unlikely canvas.
After air-dried, these three materials were chopped into 2.0-4.0 2.0-4.0ength.
Materials were chopped with a razor blade and then specifically analysed according to the following protocols (see Table 2).
These biomass materials were chopped into small pieces (1-2 cm) and dried in a hot-air oven at 105°C for 6 h.
The dried materials were chopped into small pieces and ground into fine powder form and were then extracted with a mixture of dichloromethane and methanol (DCM : ME) at the ratio of 1 : 1 [ 18].
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