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Exact(9)
No background staining was seen in untreated skin (Fig. 2g) and neither luciferase nor LacZ expression was detected in the tissue immediately below the injected skin (data not shown).
Consistent with these results, binding of IgE was high in the subconfluent Caco-2/TC7 (Figure 7C) and HCT-8 cells (Figure 7I), whereas only a background staining was seen in confluent Caco-2/TC7 (Figure 7F) and HCT-8 (Figure 7L) cells.
No background staining was seen for control C7/vIL-10.
(C) Some weak background staining was seen in control cells, compared to those over-expressing CAPN5 (D).
Very little background staining was seen in the red (Fig. 3 Bb ) or the green (Fig. 3 Bc ) channel.
Very little background staining was seen in the red (Fig. 3 Ab ) or green (Fig. 3 Ac ) channel.
Similar(51)
No staining was seen with GS-2, MPA, or PNA.
A similar pattern of staining was seen for cyclins B1 and D1, but precise quantification of the latter was not possible because of cytoplasmic background staining.
No nuclear staining was seen.
Both membranous and cytoplasmic staining was seen.
Some stromal staining was seen as well.
More suggestions(16)
background staining was achieved
background staining was examined
background fluorescence was seen
background staining was judged
background subtraction was seen
background staining was determined
background staining was produced
background staining was performed
background staining was observed
background staining was assessed
background staining was measured
background staining was done
background correction was seen
background expression was seen
background signal was seen
background staining was detected
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