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Whole brains and cerebella were excised, weighed, immediately frozen in liquid nitrogen, and then stored at −80°C for later processing.
The mucosal samples were placed in RNA later (Sigma Chemical Co., St . Louis MO, USA) and then stored at −80°C for later processing.
AM7021) at −20°C for later processing.
FNAB specimens were snap-frozen to -80°C for later processing.
Livers and muscle tissues were immediately removed and frozen in liquid nitrogen for later processing.
This data was then averaged over every 50 samples and recorded in a log file for later processing.
RNA degradation always takes place in the tissue that is removed and stored for later processing.
Evening and morning urine samples were taken for later processing.
You can even do this as a training run in preparation for later bathing, if you like.
Histological samples are taken and fixed in formalin for later processing and staining.
A number of samples were fixed in 4% paraformaldehyde (PFA) and stored for later processing for histological analysis.
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