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We use basic statistics of downscaled Global Circulation Model (GCM -projected cumulative potential GCM -projectedelecumulativeesentative potentialns.
The parameters of InSilicoTEM are summarized in Table 3 and the representative projections generated from InSilicoTEM are shown in Fig. 4B.
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Fig. 2d shows a representative projection track pathway piercing fully through the stratum corneum and epidermis – and into the upper dermis.
(A) Representative 3D projections of iWAT imaged at 12.6× magnification on the lightsheet microscope.
(B) Representative confocal projections through tail pieces fixed 48 h post-amputation following RNAi administration, stained with H3P antibody.
(B) Representative confocal projections (ten 1 μm z-stacks) of planarian head, stained with Fir1 (red), smedwi-1 (green) and DAPI (blue).
(E) Representative confocal projections through tail pieces fixed 0 h and 7 h post-amputation following RNAi knockdown of Fir1, stained with H3P antibody.
(B) Representative confocal projections through trunk pieces fixed 3 h post-amputation, labelled with runt-1 (green), Fir1 (red) and DAPI (blue).
(H) Representative confocal projections of tail pieces 48 h following amputation, labelled by Fir1 (red), smedwi-1 (green) and H3P antibody (blue).
(A) Representative confocal projections through wildtype tail pieces fixed 48 h post-amputation, labelled with Dis3l2 (red), Fir1 (green) and DAPI (blue).
(A) Representative 3D projections of iWAT harvested at indicated time points, immunolabeled by anti-tyrosine hydroxylase, and imaged at 12.6× magnification on the lightsheet microscope.
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