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However, a floating intimal membrane was visualized consistent with aortic dissection, Fig. 1.
The membrane was visualized with ECL Western Blotting Detection Reagent Pierce Biotechnologyy).
The membrane was visualized with ECL Western Blotting detection reagents (Amersham Biosciences, Piscataway, NJ).
After a further 3 washes, the membrane was visualized enhanced chemiluminescence reagents (Thermo scientific) For a loading control, the monoclonal Anti-β-actin antibody (Sigma Aldrich) in a dilution of 1∶2000 against the β-actin protein was used.
After extensive washing in TBS/Tween over more than one hour, protein on the membrane was visualized by ECL reagent (Amersham Biosciences) and exposed on Kodak Biomax MR film.
The basal membrane was visualized with viking-GFP (Flytrap).
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Signals on the PVDF membrane were visualized with an enhanced chemiluminescence kit.
After three washes in TBST, Proteins on the membrane were visualized using the enhanced chemiluminescence detection system (Amersham, Arlington Heights, IL).
The bands on the membrane were visualized using enhanced chemiluminescence method (Pierce Biotechnologies Inc .. Densitometric analysis was performed using a Bio-Rad image acquisition system Bio-Rad Laboratoriess). Bio-Rad Laboratories
Target proteins on the membrane were visualized on X-ray films by using the ECL Plus Western Blotting Detection Reagents (Amersham, Buckinghamshire, UK).
Signals on the washed membrane were visualized by autoradiography and were quantitated by densitometry analysis.
More suggestions(15)
lamina was visualized
layer was visualized
mucus was visualized
disk was visualized
barrier was visualized
membrane were visualized
membrane was studied
membrane was cleaned
membrane was used
membrane was determined
membrane was tugged
membrane was fabricated
membrane was laid
membrane was washed
membrane was designed
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