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In used experimental system, the evolution of wear scar in time is controlled by microscopy, so these precautions are easily satisfied.
Cell growth and maturation were controlled by microscopy and villin mRNA expression.
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Crack growth was controlled by optical microscopy and by progressive crack surface heat tinting.
The localization of each construct was controlled by fluorescence microscopy.
Expression of GFP-Mad2 was controlled by fluorescence microscopy.
Protein insertion was controlled by electron microscopy of freeze-fractured samples.
All participants were asked to avoid sexual intercourses 24 48 hours before the sampling visit; the date of the latest intercourse was reported and samples were controlled by optical microscopy for the presence of spermatozoa.
Wound closure was controlled by light microscopy.
All components are controlled by MetaMorph Microscopy Automation & Image Analysis Software.
Oligomeric and fibrillar forms of Aβ1-42 were produced according to [ 20] and controlled by electron microscopy.
V600EBRAF transduction efficiency was controlled by fluorescence microscopy analysing co-expression of GFP which was consistently above 90% (data not shown).
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