01/04/2023
Our luciferase mRNA was synthesized by using linear double-stranded DNA containing the T7 promoter sequence as the template, T7 RNA polymerase as the enzyme, NTPs as the substrates, and all UTPs were replaced with N1-Me-Pseudo UTP (Glycogene, Cat. No.: MR-3002) , cap1 was added for simultaneous capping during in vitro transcription to obtain luciferase mRNA with high capping efficiency. For more details feel free to contact us.
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