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One sample from a Peruvian wooden painting, (P-c containing calcite) was split into two aliquots and analysed at DCCI and GCI.
Human K3EDTA whole blood spiked with working solutions (at LQC and HQC level) were prepared and after spiking spiked sample was split into two aliquots (A and B).
The samples were split into two aliquots.
The immunoprecipitates were split into two aliquots.
Purified nucleic acid from a serum sample was split into two aliquots (DNase I-treated and untreated).
The inner part of each carbonate nodule was crushed in an agate mortar and each sample was split into two aliquots, the first treated with 2% NaOHCl solution at 60°C for 24 hours to remove any organic contamination.
Similar(20)
Methods: Leukocytes (≈108) from healthy human volunteers (n = 5) were labelled following guideline, splitted into two aliquots of 0.5 cc in plasma and saline and incubated under stirring at 37°C, for 2h and 4h.
At t0 and tfinal cells were trypsinized, harvested and each sample was splitted into two aliquots.
The sample is split into five aliquots.
The reaction mixture was split into three aliquots.
The reaction is split into four aliquots and a different dNTP is added to each aliquot.
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