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All protein expression data were expressed as mean ± standard deviation of three independent experiments.
AP-2α/β isoform: Her2 protein expression data were available for 679 tumour cores expressing AP-2α/β.
Protein expression data of a distinct set of 105 differentially expressed protein spots were examined.
Supporting documents including a photograph of the mutant phenotype, RNA and/or protein expression data, enzymatic assays, sequence alignments, etc. .
The in vivo protein expression data based on LC-MS may serve as a reference map and use for validation study for functional research on individual monocyte proteins.
Gene or protein expression data and other high-dimensional profile data with over thousands of measurements in each sample can be generated from transcriptome, proteome and metabolome studies.
All gene and protein expression data were analyzed using student t-tests or one-way ANOVAs.
Protein expression data was quantified with Quantity One Software (Bio-Rad).
µFBI and a standard bead-based assay led to identical protein expression data.
HIF-1α DNA-binding activity paralleled the protein expression data described above.
MKK3 protein expression data showed that malignant lymphoma tissues typically exhibited weak cytoplasmic immunoreactivity or were negative.
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