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cDNA was synthesized using a random hexamer primer.
Complementary DNA (cDNA) was generated from total RNA using a random hexamer primer following the protocol for Superscript II (Invitrogen, Carlsbad, CA).
500-1000 ng of RNA was reverse-transcribed with Superscript III reverse transcriptase (Invitrogen) using a random hexamer primer, as per manufacturer's instructions, while a no-RT control was set up in parallel to assess the efficiency of the DNAse treatment.
First-strand cDNA was synthesized using a random hexamer primer using the mRNA fragments as templates.
First-strand cDNA was synthesised from 1 μg of total RNA using a random hexamer primer.
First strand cDNA was synthesized using a random hexamer primer and M-MuLV reverse transcriptase.
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The purified mRNA was broken down into short fragments and was applied as a template to synthesize the first-strand cDNA using a random hexamer-primer and reverse transcriptase (SuperScript® II Reverse Transcriptase; Invitrogen, Catalog # 18064014).
cDNA was synthesized according to the Superscript III kit (Invitrogen) by using a random hexamers primer.
The total RNA of each of the virus strains was extracted using TRIZOL reagent (Invitrogen), and cDNA was subsequently synthesized using a random hexamers primer, and then standardized to 1000 ng of total RNA per sample.
cDNA was generated from total RNA using a random primer hexamer provided with the High Capacity cDNA Archive kit (Applied Biosystems, Foster City, CA).
Complementary DNA (cDNA) was generated from 5 μg of total RNA using a random primer hexamer (GE Healthcare) and aminoallyl-dUTP mix (Sigma) following the protocol for Superscript III (Invitrogen).
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