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Small bone samples were ground in a sterilized agar mortar and subject to lipid extraction in 2×1 ml CH2Cl2 MeOH (4∶1).
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Dried samples were ground with a grinding mill and sieved through a 1-mm sieve.
All samples were ground with BaSO4 (1:50) prior to measurements.
Dried plant samples were ground in a Wiley mill.
The tissue samples were ground in liquid nitrogen.
The dried samples were ground into uniform powder.
Freeze-dried ryegrass samples were ground and analyzed.
The dried samples were ground into a fine powder using a coffee grinder with stainless steel grinding chamber.
Samples were ground and homogenized using an agate mortar.
Seed samples were ground into fine powder.
Samples were ground until >90% lysis was achieved, which typically occurred after 5−10 cycles of grinding.
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