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Real-time quantitative PCR (RTQ-PCR) confirmed a subset of these changes ranging from −59% to 255% (smallest confirmation: −19%).
We confirmed a subset of phosphorylation sites by Western blot using phosphospecific antibodies, including BCAP, GAB1, and GAB2 (Figure 4).
We confirmed a subset of strain-specific SNPs by using cleaved amplified polymorphic sequence (CAPS) markers.
The rescreen identified new active series and confirmed a subset of originally observed active compounds.
We further confirmed a subset of seven selected U. gibba genes detected as under PS in our previous analysis.
We also confirmed a subset of scrapie-associated alterations identified in our microarray studies using quantitative real time RT-PCR.
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FBC searched scientific literature to confirm a subset of GAP's novel predictions, and wrote the corresponding sections.
qRT-PCR was used to confirm a subset of differentially expressed genes identified in the microarray studies.
To confirm a subset of differentially expressed genes from microarray studies, qRT-PCR was performed as previously described (Kielian et al., 2004b).
We confirm a subset of the triple contacts involving the IGF2-H19 imprinting control region (ICR) using PCR analysis for KBM7 cells.
Illumina Omni-Quad SNP data were used to determine the ethnicities of the cases and to confirm a subset of the self-reported ethnicities in the medical records of the controls.
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