“…Nature (London) 1987, 328, 596. (11) The crude transcription mixture was extracted with 1:1 phenol/ chloroform, followed by chloroform, after which the aqueous layer was loaded directly on the Mono Q HR5/5 anion exchange column (Pharmacia). The product RNA was readily separated from the NTP's by eluting with the gradient: 25-100% B in 18 min; A = 20 mM sodium phosphate/20% acetonitrile pH 6.0, B = A + 1 M KC1; flow rate = 1.0 mL/min.…”