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文献和实验Preparation of Para-magnetic beads from Promega cat#Z5482: a) suspend magnetic particles in bottle - transfer 200 ul (200 ug) of beads per sample of RNA to be purified to a microfuge tube or tubes. b) place microfuge tube
T7 Lytic Phage-Displayed Peptide Libraries: Construction and Diversity Characterization
7Select system, to construct the libraries. Using a combination of biotinylated extension primer and streptavidin-coupled magnetic beads, we were able to prepare library DNA without applying gel purification, resulting in extremely high ligation
profiling and then identify serum peptides from these proteomic profiles. We achieve the profiling analyses by using different functionalized magnetic beads to enrich specific subsets of serum proteins/peptides based on their absorption to these beads
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