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Promoter activities in each sample were visualized 2 days post-infiltration using β-glucuronidase (GUS) activity staining.
Infiltrated leaves were collected 2 days post-infiltration, and promoter activities in each sample were visualized using β-glucuronidase (GUS) activity staining.
Four-six fields per sample were visualized using x10 objective.
16 gel bands of salivary gland homogenate sample were visualized after silver staining.
The methylated and unmethylated band intensities of each sample were visualized and measured using Storm840 and ImageQuant Software (Amersham Biosciences, Little Chalfont, UK).
PCR products (1.5 μl per sample) were visualized by gel electrophoresis using GelRed™ (Genaxxon bioscience GmbH, Ulm, Germany) to stain the DNA.
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Spatially-resolved differences in the topography of the coated sample are visualized upon prolonged incubation with chloride-containing electrolyte, thus allowing to assume a direct evidence of chloride ion permeation through the polymer matrix simultaneous to water uptake.
In order to illustrate the tumor LOH information from several samples the virtual probes with tumor LOH information from at least one sample are visualized using the DIGMAP software [21].
After Illumina standard quality control filtering, read quality for each sample was visualized using FastQC version 0.10.0 (Andrews 2010).
Immunofluorescent samples were visualized with an inverted DMI 400CS confocal microscope (Leica, Germany).
The IL-6 and NF-κB samples were visualized using a Novo Link Polymer Kit (RE7280-K, Leica Microsystems, Tokyo, Japan).
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