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Obtain ultra-high purity genomic DNA within 1 h from cells and tissues
A powerful probe-based qPCR master mix that supports primers and probes premixing and multiplex amplification.
The dsRNA sequence synthesized by UTP modified in vitro transcription is intended to be used as a standard for dsRNA residue detection.
10 - 250 kDa prestained; Three-color protein marker
The ideal choice for site-directed mutagenesis.
One-step developing and fixing, simpler operation, faster and more efficient
