Exact(5)
LRRK2 autophosphorylation and 4E-BP phosphorylation were detected by autoradiography using a phosphor screen, scanned on a STORM 840 scanner (GE Healthcare, Piscataway, NJ, USA), and quantitated using IMAGE J software (NIH).
TLC sheet were developed in 1.2 M LiCl and 0.1 mM EDTA, exposed to Fuji BAS phosphor screen, scanned using Fuji Phosphor Imager and quantified by image gauge software.
The arrays were exposed to a low-energy phosphor screen (Molecular Dynamics, Sunnyvale, CA) for 5 days, the screen scanned (Phosphorimager 860, Molecular Dynamics), and pixel intensities quantified using ImageQuant (Molecular Dynamics).
Gels were exposed to a PhosphorImager screen, scanned using a Typhoon PhosphorImager, and quantified using ImageQuant software (GE Healthcare, Waukesha, WI).
The membranes were exposed to a Storage Phosphor Screen, scanned (Storm, GE-Healthcare, USA) and the signal was quantified using Image Quant (GE-Healthcare, USA).
Similar(55)
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All blots were exposed to PhosphoImager screens, scanned and quantified using a Typhoon 9400 PhosphoImager (Amersham/GE Healthcare).
The membranes were exposed to PhosphorStorage screens, scanned with a PhosphorImager (Molecular Dynamics) and quantified using the ImageQuant software.
After drying, TLC plates were exposed to C-sensitive screens and the screens scanned with an FLA-3000 denscannerric scanner (Fujifilm, Düsseldorf, Germany).
Gels were dried, exposed to a storage phosphor screen for 6-12 hours, and the screens scanned using a phosphorimager (Molecular Imager FX, BioRad).
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