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Blots were then visualised with a STORM 840 (Molecular Dynamics, Sunnyvale, CA, USA).
The blots were then visualised using enhanced chemiluminescence (Amersham, Bucks, UK).
The blots were then visualised with an ECL kit (Amersham Life Science, Piscataway, NH, USA) and exposed for 30 s (NPM) and 1 min (PCNA, GAPDH) to X-ray film.
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The predicted land use changes were then visualised using photorealistic image rendering software.
The BrdU and FISH probe signals were then visualised simultaneously by incubating with the appropriate antibodies.
The proteins were then visualised with Coomassie brilliant blue staining.
Gels were then visualised under UV light (254 nm).
RNAs and microtubules were then visualised with total internal reflection (TIR) microscopy.
Protein products were then visualised by chemiluminescence (NEN Life Science Products, Boston, MA, USA) and autoradiography.
The previously calculated relative rates of these regions were then visualised with histograms and radar plots.
Samples were then visualised using a Jeol Jem 100-s electron microscope.
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