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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.
Rapid, Reliable, and Versatile cDNA Synthesis for qPCR
An ultra-fast workflow based on enzymatic fragmentation to prepare DNA libraries for mNGS
Obtain several bacterial samples (gram-negative and gram-positive bacteria) genomic DNA within 30 min
Upgraded high-fidelity PCR Master Mix with ultra-fast amplification
10 × Transcription Buffer is a reaction buffer optimized for in vitro transcription with T7 RNA Polymerase (Vazyme #GMP4101PB).
Kits for performing Direct PCR on Plant leaf/Plant seed
