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Enzymatic fragmentation-based fast DNA library preparation kit for Illumina
One-Step RT-qPCR mix are in one tube, and support multiplex detection
MGI platform capture universal blockers and post-PCR primer mix
Single-cell transcriptome amplification using 1 - 1000 cells or 10 pg - 10 ng RNA as template
Manually extract microbial DNA from various of biological fluid samples
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.
