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By using the tag correlation dictionary, 47 tags were validated.
Those UMCs that most closely matched the PMT tags were validated as Accurate Mass and Time (AMT) tags; moreover, this technique provided a list of peptides observed and an abundance value for each.
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For all of the constructs, the polarity of the HA tags was validated by immunofluorescence in multiple independently transfected cell clones.
The specificity of V5 tag was validated by IHC using V5 antibodies and Baf250a antibodies (Supplementary information, Figure S2C).
Measures from the Hi-Tag system were validated by comparing values with those from a single human observer, using observations from three 2-h intervals from 35 Holstein calves and heifers aged 4, 6, and 9 wk and 3, 6, and 9 mo, respectively.
The results of DGE-tag profiling were validated by examining gene expression in a subset of genes using RT-qPCR.
Measures from the Hi-Tag electronic system were validated by comparing values with those from a human observer for fifty-one 2-h observation periods from 27 Holstein cows.
The NZ9000 SEC-BLG NZ9000 SEC-BLGuced with nistrainnd rBLG expression and secretion wase valinducedby withernisintting with andanti-6x His-tag Ab.
Only ten were validated.
Positive results were validated.
Three of the cellular targets of these ribozyme sequence tags have been validated.
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