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For highly specific and sensitive genotyping without optimization requirements
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.
TGS Fast DNA library preparation kit based on ligation for Nanopore sequecing
Upgraded prokaryotic rRNA removal kit covering more species and reducing residual rRNA.
MGI platform RNA library preparation matching special adapter; providing 96 different single indexes markers
One-step developing and fixing, simpler operation, faster and more efficient
