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Bands were detected when RNAP + σE or σH were applied (Fig. 3b).
In all cases, appropriate controls were performed to demonstrate that no bands were detected when the OE RNA was not reverse transcribed.
As a contrast, no bands were detected when the supernatant of P. acnes cultures was immunoreacted to anti-GFP antiserum (Figure 1F, right panel).
In contrast, multiple bands were detected when the probes were allowed to bind to nuclear extracts from dox-treated cells.
No bands were detected when using neutral glycolipids isolated from the rest of the analysed cell lines (BT474, SKBR-3, T47D, and MCF-7).
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In contrast, no protein band was detected when leaf extracts from "vector control" tobacco (Fig. 3D).
In contrast, no band was detected when the membrane was blotted with normal serum as a negative control (Fig. 5A, lane 2).
A monomer band was detected when no SDS was mixed with the protein.
No band was detected when Methods B and C were used to amplify the EGFR gene (data not shown).
A 70 kDa band was detected when the SW626 supernatant was stained with the anti-CD55 mAbs BRIC216 and BRIC230.
As shown in Supplementary Figure S3A, the cleaved caspase-8 band is detected when WT caspase-8 is overexpressed; however, it is undetectable when caspase-8 C377A is overexpressed.
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