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The protein band was visualized using X-ray film.
The reacted protein band was visualized using the ECL chemiluminescence detection system (Amersham).
After further washing, immunoreactive band was visualized using NBT-BCIP as a chromogenic substrate for alkaline phosphatase.
Protein band was visualized using ECL and Kodak film.
The proteins were separated on the NuPage 4 12% gel (Invitrogen, Carlsbad, CA) and the band was visualized using either Lumina Classico or Crescendo Western HRP substrate system (Millipore) depending on the signal intensities.
Each band was visualized using enhanced chemiluminescence Western blotting detection reagents (GE Healthcare Life Sciences, Barrington, IL, USA), and the chemiluminescence was detected using LAS-4000 (GE Healthcare Life Sciences).
Similar(52)
DNA bands were visualized using a UV (254 nm) illuminator.
The bands were visualized using ECL Chemiluminescent Substrate Reagent (Amersham).
Bands were visualized using LI-COR Odyssey machine.
Individual protein bands were visualized using an Odyssey imager (LiCOR).
Protein bands were visualized using Coomassie brilliant blue stain.
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