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This demonstrates the ability of the probe to connect local information to the global behaviour and structure of the flow.
The reaction of methanol to dimethyl ether on zeolite HZSM-5 was used to demonstrate the ability of the probe to study heterogeneous catalysis reactions in situ.
In addition, the ability of the probe to detect Ca2 + in living cells (HeLa cells) via an enhancement of the fluorescence has also been demonstrated.
A comprehensive analysis of the recognition ability of the probe towards metal ions was conducted by ultraviolet absorption and fluorescence emission spectroscopy.
In addition, the ability of the probe to detect thiophenols in living cells (HepG2 cells) via an enhancement of the fluorescence has also been demonstrated.
Therefore, we hypothesize that the repeated As in the regulatory domain influenced probe stability and further impacted the ability of the probe to assay the targeted sequences in the salt solution.
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We first tested the ability of the probes to detect a synthetic oligonucleotide target.
The sensing abilities of the probe towards various anions were studied by absorption and emission spectroscopies in dimethylsulfoxide (DMSO) as well as in DMSO/H2O.
The ability of all the probe sets of the Affymetrix Genechips to hybridize to their target mRNAs was ascertain using the ADAPT database [ 32].
To extend our analysis of PR-dependent gene expression in FTE and HGSC, we tested the ability of these probe sets to predict a given sample category using a shrunken centroid classification methodology (Tibshirani et al. 2002; results shown in Table 1).
The discrimination ability of these probe sets was assessed by a multidimensional scaling (MDS) assay.
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