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Blots were probed with green fluorescent protein (GFP) antibody.
Blots were probed with antibodies against p62, GFP, and β-actin.
Blots were probed with HRP-conjugated secondary antibodies (Jackson).
Western blots were probed with an antibody recognizing Akt phosphorylated Ser473 (Cell Signaling, Beverly, MA).
Western blots were probed with rabbit anti-FimA sera and HRP-linked anti-rabbit IgG.
Blots were probed with antibodies specific for ADH1 and ADH4, respectively.
The blots were probed with FAT/CD36 antibody (Cascade Biosciences) and visualized as described above.
These blots were probed with N intracellular (NI; [18]) or hsp 70 antibodies (Sigma).
Proteins of interest on the blots were probed with specific antibodies.
The blots were probed with indicated primary antibodies, followed by secondary antibodies conjugated with HRP.
Blots were probed with an antibody specific to the phosphorylated Ser51 residue of eIF2α (BIOSOURCE International).
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blots were imaged with
blots were revealed with
blots were stripped with
blots were hybridized with
blots were analyzed with
blots were rehybridised with
blots were normalized with
blots were generated with
blots were treated with
blots were reacted with
blots were washed with
blots were blocked with
blots were visualized with
blots were developed with
blots were performed with
blots were quantified with
blots were reprobed with
blots were processed with
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CEO of Professional Science Editing for Scientists @ prosciediting.com