The Universal RiboClone® cDNA Synthesis System contains the reagents required for synthesis of double-stranded cDNA from mRNA and subsequent ligation into a suitable vector. The system is based on the method described by Okayama and Berg with modifications by Gubler and Hoffman. First-strand synthesis is driven by AMV (Avian Myeloblastosis Virus) Reverse Transcriptase and either Random Primers or Oligo(dT)15 Primer, followed directly by second-strand replacement synthesis using RNase H and DNA Polymerase I. After treatment with T4 DNA Polymerase to flush the ends, the double-stranded cDNA molecules are prepared for cloning by size fractionation and addition of EcoRI Adaptors. The resulting cDNA preparation then can be cloned into a suitable vector.
Store control RNA at –70°C. Store Sephacryl® S-400 at 2–10°C and Spin Columns at room temperature. Store other components at –20°C.
For product intended use please see Patents & Disclaimers tab.
C4360, C1101, C1181, C1281, C1291, C1381, V3181 For Research Use Only. Not for Use in Diagnostic Procedures.
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