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With the co-culture method we described, the interactions for more than one species can be measured in one experiment.
The RNA capture/QPCR method we described here can be used for quantifying the expression ratios of alternatively spliced mRNAs from a single gene or for direct comparison of expression of different genes.
γFe2O3 NPs were prepared according to the method we described previously [12].
As in the simplest method we described in Section 2.2, we generate a hypothesis in the form of a set of samples considered for removal one by one.
Ventilation performance were analysed using a new analysis method we described in a previous study which takes into account ventilation variability.
Importantly, using this method, we described the expression dynamic patterns of several genes, especially OsPINs, during the rice LRP development for the first time.
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The method we describe here offers a novel approach for fabricating high quality, three-dimensional organic structures.
The method we describe could be useful for studies in mice of antisense or ribozyme inhibitors targeting the IRES as well as other RNA biochemical studies in vivo.
The iPS cell derived EBs are stimulated by Wnt10b one day before transplantation of multiple EBs in vivo (a method we describe as the clustering-dependent embryoid body (CDB) transplantation method).
However, the method we describe here could equally well be used to determine cell phenotypes from brightfield and darkfield images from traditional microscopy provided the ground truth is measured using the same microscopy platform.
So, in the case of binary fingerprints, the only distinct profile similarity method we describe is BAYES method (Equation 24).
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