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PTEN expression was evaluated by immunohistochemistry on tissue microarrays consisting of multiple cores of 133 resected stage II pancreatic ductal adenocarcinomas.
EXPERIMENTAL DESIGN: We examined the expression of MAP4K4 by immunohistochemistry using tissue microarrays consisting of 66 stage II PDA and their paired benign pancreatic tissue.
Pioneering studies relied on microarrays consisting of both strands of the targeted genomic regions [2], [15], [16].
Using microarrays consisting of 18,664 probes we compared gene expression profiles of LCLs from SZ cases and healthy controls.
Human cDNA microarrays consisting of ∼43,000 elements were obtained from the Stanford University functional genomics facility [58].
We hybridized 21 microarrays, consisting of three biological replicates, for all 7 genotypes, to determine if transcript accumulation 24 h after treatment with MJ differed among the genotypes.
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Microarrays consist of a number of probes that bind messenger RNA from specific genes (mRNA is the linking molecule between a gene and the protein it encodes).
The units of microarrays consist of needle-like VO2 particles with a mesoporous structure, in which crack-like pores with a pore size of about 2 nm and depth of 20 100 nm are distributed on the particle surface.
The basic probe pattern on the microarrays consisted of two PC, six NC, and four CK, which could be used as the position reference and landmarks for image analysis.
The 8 CR microarrays consist of 6 microarrays from individual samples and 2 microarrays each produced using pooled RNA samples from 3 other individual mice.
The microarrays consist of the expression data for the tissues associated with colon, blood, lung, breast, prostate, and cancer of the central nervous system.
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