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b1 and b2 represent the bright-field and fluorescence microscopy pictures of group B bacteria, respectively.
Typical polarizing optical microscopy pictures of the microemulsion samples (Figure S3).
c1 and c2 represent the bright-field and fluorescence microscopy pictures of group C bacteria, respectively.
As shown in Fig. 4, a1 and a2 represent the bright-field and fluorescence microscopy pictures of group A bacteria, respectively.
Fluorescence microscopy pictures of E. coli, S. aureus and Y. enterocolitica, control (left two column figures) and β-casein 197 treated (right two column figures).
Fig. 5 Transmission electron microscopy pictures of the fibre based matt test photographs step 5 at × 150 k (scale bar measures 100 nm).
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d Microscopy picture of one central sensing region with an onsite heater highlighted with red frame.
c Microscopy picture of one central circular sensing region without local heater.
b SEM of an La0.7Sr0.3MnO3 triple nanoconstriction (reproduced with permission of [31]) Fig. 12 a An electron microscopy picture of a typical microbridge.
The scanning electron microscopy picture of the secondary explosion residue exhibited a higher degree of fragmentation and a more developed pore structure.
It can be decreased and can even change its sign in the bridges with widths of 1.5 and 1.0 μm under magnetic field of 1 T. Figure 12a shows an electron microscopy picture of a typical La0.7Ca0.3MnO3 microbridge patterned by EBL [33].
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