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The dsRNA sequence synthesized by Pseudouridine-UTP modified in vitro transcription is intended to be used as a standard for dsRNA residue detection.
The dsRNA sequence synthesized by N1-me-pseudo-UTP modified in vitro transcription is intended to be used as a standard for dsRNA residue detection.
This kit employs double-antibody sandwich ELISA to detect the residual double-stranded RNA (dsRNA).
A next-generation T7 RNA polymerase engineered to minimize dsRNA byproducts by up to 100×, enabling safer and more efficient mRNA therapeutics.
qPCR standard kit
Developed specifically for multiplex PCR
