To rule out the possibility of sequence polymorphism at primer binding sites, further PCR experiments were undertaken using alternative primers designed to anneal at highly conserved sequence stretches in both pfhrp2 and pfhrp3.
To identify the amino acids involved in hippuristanol binding, a series of NMR experiments were undertaken in which 1H-15N-HSQC spectra of uniformly labelled eIF4AI-CTD were obtained in the absence or presence of compound (Fig. 1A).
Further spectroscopic experiments were undertaken to obtain information on the potential location of the HSA binding site of CTN.
Solvent extraction experiments were undertaken at 27 ± 0.5°C.
With the new architecture, electrochemical measurement experiments were undertaken.
The experiments were undertaken using a water channel.
Objective and subjective experiments were undertaken to evaluate the presented methods, as summarized in Table 1.
Animal experiments were undertaken according to the Guidelines for Animal Care and Use Committee, Kyushu University (Fukuoka, Japan).
To justify the proposed system, subjective listening experiments were undertaken in an anechoic room.
Extensive experiments were undertaken to verify the derived algorithm, with border effect, via realistic mobility traces.
