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Fig. 2. Selective ablation of BRG1 in the surface ectoderm and epidermal keratinocytes of K14-Cretg/0/Brg1L2/L2 fetuses. (A) Immunohistochemical (IHC) detection (green fluorescence) of Brg1 (a-h) on E11 forelimb (a,b,e,f) and hindlimb (c,d,g,h) bud tranverse sections from control (a,c,e,g) and Brg1ep-/-(c) (b,f,d,h) fetuses. Superimposition of Brg1 (green fluorescence) and DAPI staining of nuclei (blue fluorescence; e-h). Scale bar in a: 24 µm. (B) IHC detection of Brg1 on transverse sections through the dorsal ectoderm of E12.5 Brg1L2/L2 (control; a,c) and Brg1ep-/-(c) (b,d) fetuses. Superimposition of Brg1 (green fluorescence) and DAPI staining of nuclei (blue fluorescence; c,d). Scale bar in a: 24 µm. (C) IHC detection of Brg1 on dorsal skin sections from (a,b) control Brg1L2/L2 and (c,d) Brg1ep-/-(c) E18.5 fetuses. Red staining corresponds to BRG1 antibody and blue staining to DAPI. E, epidermis; D, dermis. The dotted line indicates the dermal-epidermal junction. Scale bar in a: 10 µm. (D) PCR detection of the Brg1 L2 and L- alleles in the epidermis and dermis of E18.5 fetuses. DNA was extracted from tail epidermis (E; lanes 1,3,5,7,9) or dermis (D; lanes 2,4,6,8,10) of fetuses with the indicated genotypes, isolated from females that were Tam treated from either E9.5-E13.5 (lanes 3,4) or E12.5-E16.5 (lanes 5-8), or oil (vehicle) treated from E12.5-E16.5 (lanes 9,10).





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