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文献和实验Real-Time qRT-PCR standard curves... efficiency is too h
/melting data. -YuJ- Hi YuJ, Could you please describe how you preparing your quantitative standard? Thanks Hadrian -Hadrian- Hi Hadrian, My quantitative standards are prepared as such... 1. RNA isolation using TRIZOL
Increasing Sensitivity in Northern Analysis with RNA Probes
between single-stranded RNA and double-stranded DNA probes are not significant. ULTRAhyb is now a part of every NorthernMax™ Kit that Ambion sells. Using RNA probes in Northern analyses results in significantly greater sensitivity as compared to double-stranded
E.Z.N.A.® HP Total RNA Kit Spin Protocol Eukaryotic Cells and Tissues
before RNA isolation. b. OBI DNase I digestion buffer is supplied with OBI RNase-free DNase set. c. Standard DNase buffers are not compatible with on-membrane DNase digestion. 2) Pipet 75 ul of the DNase I digestion reaction mix directly
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