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Overview
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This is an engineered T7 RNA polymerase variant (low dsRNA) derived from the wild-type T7 RNA polymerase and produced in Escherichia coli. It significantly reduces the production of double-stranded RNA (dsRNA) while efficiently incorporating cap analogs, and exhibiting highly efficient in vitro transcription (IVT) comparable to the wild-type T7 RNA polymerase. It catalyzes the 5'→3' synthesis of RNA on double-stranded DNA from its T7 promoter sequence (5'-TAATACGACTCACTATAG*-3') and uses NTPs as substrates.
Note: G* is the first base of the RNA transcript.
Feature
• dsRNA level lower to about 1/100000
• Comptiable with Trilink CleanCap AG
• High yields comparable to WT
• Lower Cap input
• Animal origin-free (AOF)
Unit Definition: the amount of enzyme required to incorporate 1 nmol of [³H] GMP into the acid-insoluble precipitate within 1 hour at 37°C and pH 8.0 is defined as 1 unit.Please contact us at for specific academic pricing.
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Overview