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Samples positive in both tests were tested for HCV RNA by using qualitative reverse transcriptase polymerase chain reaction (PCR) amplification of the 5' non coding region, as previously described [13], [21], [22].
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Antioxidant activity was determined by using qualitative and quantitative methods.
The data was analysed by using qualitative coding, and categorising information according to key themes.
The data were analysed using qualitative content analysis [ 23], assisted by a computerised qualitative data analysis program, QSR NVivo7 [ 24].
Qualitative data were analyzed using qualitative description.
Reverse transcription (RT) was carried out by using a reverse transcription kit (Applied Biosystem).
Total RNA was reverse transcribed by using Maxima reverse transcriptase mix (Fermentas).
The RNA (1 mg) was reversed to cDNA by using a Reverse Transcription Kit (Takara).
Total RNA from C. cladosporioides MD2 was reverse-transcribed by using SuperScript III Reverse Transcriptase (Invitrogen, California, USA) and oligo dT 18.
Reverse transcription was performed by using a TaqMan Reverse Transcription Kit (Applied Biosystems).
Reverse transcription was conducted by using SuperScript® III Reverse Transcriptase (Invitrogen, Grand Island, NY, USA).
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