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A 2D CT (constant time -HSQC experimentime -HSQC thexperimentsonances foresolvedven proline residues.
A 2D CT-HSQC experiment resolved the Hδ-Cδ resonances of wild-type FKBP12 for the major slow exchange state of all seven proline residues and for the minor slow exchange state of Pro and Pro (Supplementary Figure S1 at http://www.biochemj.org/bj/453/bj4530371add.htm).htm
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However, none of the experiments resolved the problem.
Comparative real-time PCR experiments resolved the glycolytic genes into three sub-sets based on their expression profiles during development.
High-resolution mapping following up with knockout and allele replacement experiments resolved the QTL into the underlying genes (AMN1, RGA1, FLO1, and FLO8) or even into the causative nucleotide.
Observing three distinct water clusters in the same experiment resolves long-standing questions about their relative stabilities.
The origins of migration remain in the realm of pure conjecture; neither observation nor experiment has resolved the matter.
30 μl of each experiment were resolved by SDS-PAGE, gels were Coomassie brilliant blue stained, dried and exposed to Kodak X-Ray films for 72 h.
To determine which peptides supported platelet or D1D2 binding, data from each experiment was resolved into responders and nonresponders as follows.
These experiments therefore resolved several important issues.
Reaction mixtures from either full-length or VPg-nonanucleotide substrate experiments were resolved via 13.5% Tris-tricine PAGE analysis.
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