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The detection limits of PCR & qPCR for bacterial 16S rRNA were next assessed using Escherichia coli DNA samples extracted from a known bacterial titer.
Because S-MB predominately formed dimers in the above SDS-PAGE (see above), potential 3D-interactions between S-MB monomers were next assessed with several docking algorithms.
The strains were next injected intravenously in mice and tissue burden were next assessed from kidneys and spleen from sacrificed animals (Fig. 8).
Both the molecular weight (MW) and self-aggregation properties of MB and S-MB peptides in a lipid-detergent environment were next assessed in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) experiments.
Comparison of genomic aberrations suggested a correspondence between proteomic classes of EGFR, NF1 and PDGF and the corresponding TCGA transcriptomal classes, therefore expression levels for genes encoding the core proteins (total forms) were next assessed in each of the four transcriptomal clusters.
Specific effects on T-cell function were next assessed.
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This protective effect was next assessed at the histological level.
Output was next assessed relative to associated disease prevalence.
IFN-γ was next assessed in vaccinated mice after challenge.
Correlation between DC aggregation and synaptic distribution was next assessed.
The ability of HA to affect breast cancer cell colonization and tumor growth within the bone microenvironment was next assessed.
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