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One microgram isolated total RNA was DNAse treated (Promega) and used as template to generate complementary DNA (cDNA) utilizing a random hexamer primer [p dN 6] and MMLV reverse transcriptase (Promega).
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To obtain first strand cDNA pools, reverse transcription was carried out using SuperScript IV (Thermo Fisher Scientific) with a random hexamer and oligo dT primer, following the manufacturer's instructions.
cDNA was synthesized using a random hexamer primer.
One microgram of total RNA was reverse transcribed with avian myeloblastosis virus reverse transcriptase (Promega, USA) and a random hexamer.
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 synthesis was synthesized with a random hexamer and SuperScript II (Life Technologies Corp., Carlsbad, CA).
First strand cDNA was synthesized using a random hexamer primer and M-MuLV reverse transcriptase.
The synthetic library was amplified with three commercially available DNA polymerases using an anchored primer with a random 3' hexamer end.
For cDNA synthesis, RNA (5 μL), a random hexamer, and a SuperScript III Kit (Invitrogen, Carlsbad, CA, USA) were used.
cDNA was reverse transcribed using a cDNA Synthesis Kit (BioLine, London, UK) with a random hexamer primer mix.
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