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By using serial chimerism analysis, impending hematological relapse could be detected in advance to allow time to collect cells from the donor for DLI.
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We could extend the idea of motor control by using serial communication.
Positive samples were quantified by using serial dilutions.
These values were determined by using serial sections with Hoechst nucleus staining.
A standard curve was generated by using serial dilutions of CaCO3.
In brief, the risk of relapse was assessed using serial blood chimerism assays (weekly until day+100, monthly until first annual visit and then yearly).
Numbers of viable bacteria were estimated by limiting dilution using serial ten-fold dilutions of samples.
All assays were performed in duplicate and by the standard curve method using serial cDNA dilution.
Efficient partition of hybrid meshes has been accomplished by transforming them to suitable graphs and using serial graph partitioning algorithms.
Exact quantification was achieved by serial dilution with cDNA produced from total RNA extracts using serial dilution steps.
Using serial section, intra-hepatic PD1 and PD-L1 expression was also detected dynamically by immunohistology.
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