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文献和实验with most enzymatic recations, if you're going to be making cDNA, etc., you'll not want to use TES. If you've done a good job on the purification, your RNA will be stable at -20 without the SDS. Ann Sluder
Sauer:RNA Purification from E. coli
too low in RNA prep''d by resuspending E. coli in tri-reagent (called Trizol from here on) as the "lysis" step. Even though Trizol has phenol and guanidinium thiocyanate, and the samples were heated to 65 degrees for 30 minutes, the large RNAs just didn''t
Rapid System for Evaluating Bioproduction Capacity of Complex Pharmaceutical Proteins in Plants
RNA sites, silencing, and product compartmentalization on product yield and quality, researchers still cannot reliably predict which proteins will be produced at high levels or what manipulations will guarantee enhanced productivity. We have optimized
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