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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.
Developed specifically for multiplex PCR
Upgraded version of small RNA library preparation kit, compatible with lower sample input volume; better effect of library preparation for special samples
Single-cell transcriptome amplification using 1 - 1000 cells or 10 pg - 10 ng RNA as template
Show the Mycoplasma some "colors"
qPCR standard kit
