Suggestions(4)
Exact(1)
After electrophoresis and Western blotting on PVDF membranes (Immobilon-P; Millipore, Bedford, MA, USA), the blots were processed by SNAP i.d.™ Protein Detection System (Millipore) as described by the manufacturer instructions.
Similar(59)
Western blots were processed, scanned and analysed by densitometry as previously described [ 16].
Control blots were processed without incubation of the primary Ab.
All the blots were processed with ECL Plus Western Blotting detection kit (GE Healthcare, Piscataway, NJ, USA), and the signal was detected by a Typhoon 9410 Variable Mode Imager.
Lysates were immunoprecipitated (2 hr), washed 4 times with NP-40 buffer and were processed by Western blotting.
Equal amounts of cell lysate were processed by Western blotting.
Then, cells were processed by Western blot analysis using specific antibodies against Ras-GRF1 and Ras-GRF2 proteins (Fig. 3A and C).
Dot-blots were processed for antibody signal detection similar to the Western blot strips.
Validation by western blotting was processed using the pooled and individual mitochondrial samples in both PBC mouse model and control groups at different time points.
The immunoblot was processed by chemiluminescence detection (Chemiluminescence Blotting Substrate [POD], Roche Molecular Biochemicals).
Blot image files were processed with MultiGauge (FujiFilm Lifescience).
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com