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The fact that berry cultures derived from berry explants in different stages of development yielded protein expression patterns that could be matched to expression profiles found in berries provide an excellent platform for further studies, also on the metabolite level.
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From these 89 clones, 46 clones could be matched to the SAGE expression data [ 19].
These expression signatures may then be matched to their corresponding sequence in the genome to delineate gene expression.
"1" is representative of the respective organ(s) presence within the respective homeotic mutant, and "0" represents the organ(s) absence/diminishment. Organ occurrences were matched to transcript expression levels "1" = leaf or root expression < transcript expression and >4TPM, "0" = transcript expression = 0 TPM to determine organ enriched gene expression.
qRT PCR analysis data were matched to protein expression levels studied by immunohistochemistry scores.
qRT PCR analysis data were matched to protein expression levels studied by Western blot analysis and immunohistochemistry.
Thus, Myc protein levels in immune-activated T cells are matched to high expression of amino acid transporters and to high rates of amino acid uptake.
The increased production of (E -caryophyllene was matchE -caryophyllened expression of the corresponding TPS gene.
First, genes in the 117 GISTIC regions (n = 1,750) were matched to available gene expression data (n = 1,078) and correlated across tumor samples as previously described [ 25].
Real-time quantitative RT PCR analysis data were matched to the protein expression values in the 2-DE analyses, immunofluorescence analyses, and immunohistochemistry analyses.
A subset of ESTs were matched to microarray probes and expression was measured under 12 different conditions.
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