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One set of samples emits violet light (around 400 nm), while the other set of samples grown under higher substrate temperature emits green light (around 520 nm).
The other set of samples was cultured quickly after collection.
The other set of samples was kept with PBS instead of GSH, to obtain the amount of receptor that was either degraded or shed from the cell surface.
The other set of samples was stored at −70° C for future biochemical analysis/bio-assay.
The other set of samples were collected from Kulongjiang Chimney at Qimen in Anhui province.
After resuspending in water and addition of internal standards (UC-Tyr and UC-Phe, 100 pmol each), the other set of samples was subjected to acid hydrolysis (6 M HCl for 24 hr at 110°C).
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Likewise, the proposed models, constructed with 700 measurement samples, show good results when applied to other sets of samples (i.e., second campaign previously described).
Our goal was to identify potential biologically important differences that should be tested in other sets of samples and with additional methods.
Other sets of the samples consisting of the MNCM solid films were deposited on silica substrate by means of the small amounts of the mentioned C1, C2, and C3 solution evaporation.
Telomere lengths calculated from the two sets of replicates shown were averaged with telomere lengths from four other sets of replicate samples from similar experiments to give the numbers shown, ± standard deviation.
For the primary analyses, we also analyzed two other sets of combined samples: AGP trios together with AGRE families; AGP trios together with unrelated SAGE controls; and all three data sets.
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