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An additional explanation is that expression levels in brain may be too low to detect using microarrays, but were detectable in our normalised cDNA library of hippocampus.
However, FACS analysis indicated phenotypically differing CD11c Langerin+ populations in the epithelium (CD11b(low)CD103(low)) versus stroma (CD11bCD103 low)). Additionally, corneas from huLangerin-DTA mice were devoid of Langerin+ cells in the epithelium but were detectable in the stroma.
There were, however, also genes where the differential expression in response to LPS appeared markedly different between monocytes and PBMC, but were detectable in both samples.
EMA, MMA and α-KGA were undetectable in plasma but were detectable in urine.
Based on The semi-quantitative expression analysis revealed PtoWUSa and PtoPWOX4a were strongly expressed in the CAM zone, but were detectable in other examined tissues.
There were additional 71 miRNAs that were significantly present (|ΔCt|⩾3) but were detectable in <50% of the LOS or SOS group (Supplementary Table 3).
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This truncated protein might be too low in abundance or too unstable to be detected in a western blot, but was detectable in fixed tissue using enhanced signal detection protocols.
FUL was not detected in the root, but was detectable in vegetative shoot organs (stem and leaf) and was highly expressed in flower and particularly fruit.
Epicatechin was not detected in either variety until véraison, but was detectable in Norton at 85 and 99 DAB as well as in Cabernet Sauvignon post-véraison.
Oxygen was not detected during heating of the natural jarosite clay but was detectable in the ferric sulfate hydrate experiments at temperatures at and above 600°C (Fig. 4).
Autoantibodies (AABs) against platelet antigens are considered as the diagnostic hallmark of ITP, but are detectable in only 50% of patients.
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