Although primer module cooS-1F, cooS-3F, and cooS-3R did not produce detectable products from any of the templates analyzed in this study, each of these primer modules amplified cooS genes from gut communities of phylogenetically-higher termite species in a subsequent study (manuscript in preparation).
All fMRI data were spatially normalized to a common template and analyzed at the individual and group levels with statistical parametric and nonparametric methods.
Using thermal evaporation, we fabricated five uniform and regular arrays of Ag nanostructures with different shapes that were based on an anodized aluminum oxide template and analyzed their optical properties.
The HA powder obtained from co-precipitation during the synthesis (not attached to porous template) was analyzed by XRD and Raman spectroscopy, and its morphology/crystalline structure was determined by TEM. Figure 2a shows the XRD spectrum of the HA powder sample obtained with the method discussed above.
The sequences of the ESTs (with vector sequence trimmed off, as recombinant plasmids were used as template) were analyzed for their homology against the publicly available non redundant genes/ESTs/Transcripts in the NCBI database using the BLASTN and BLASTX algorithms [85], [86], [87], [88].
The three types of template were analyzed separately by combined bisulfite restriction analysis (COBRA).
The amplified template was analyzed using the MultiNA Microchip Electrophoresis System DNA-500 kit (Shimadzu Corp., Tokyo, Japan).
For a given cluster, the multiple sequence alignment pertaining to the respective cluster and two-protein alignment between the query and modeling template were analyzed.
Selected articles were reviewed and relevant information was extracted into a standardized template and analyzed for key cross-cutting themes, ie, impact of technology on costs, factors influencing this relationship, and methodological challenges in measuring such linkages.
Since slightly green colonies growing on chloramphenicol suggested the presence of the starting BAC template, we analyzed colonies without color and that were unable to grow on LB Kan plates for the presence of the desired B5R or A33R BAC recombinant.
