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The supernatant was transferred to sterile tubes for storage and it was kept at −18 °C.
Plasma was separated within 15 minutes of blood collection, and aliquots were transferred into trace element-free Eppendorf plastic tubes for storage at −20°C.
The filled silastic implants were rinsed twice with 95% ethanol and once with sterile water, left to airdry at room temperature, and packed in 1 ml sterile plastic tubes for storage.
Aliquots of plasma and PRP were dispensed in Eppendorf tubes for storage at -70°C.
The aliquots were divided over 4 trays of 96 tubes for storage in the freezers.
The tissues were cut into 5 g pieces and inserted into 50 ml polypropylene tubes for storage (Cornig, NY, USA).
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A flexible liquid crystal display that may lead to screens that roll up into a small tube for storage was announced this week.
Supernatant was then separated and transferred to a new centrifuge tube for storage at −20°C until further use.
Prior to analysis, entire leaves were crushed with a mortar and pestle and each transferred to a 2 mL microcentrifuge tube for storage.
Prior to analysis, entire leaves were ground with a mortar and pestle and transferred to a 2 mL microcentrifuge tube for storage.
At maturity, each plant was dried and its seeds were sifted through a coarse mesh to remove plant debris before being placed in a plastic tube for storage.
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