FIGURE
            Fig. S8
- ID
 - ZDB-FIG-170901-19
 - Publication
 - Gau et al., 2017 - An ancient neurotrophin receptor code; a single Runx/Cbfβ complex determines somatosensory neuron fate specification in zebrafish
 - Other Figures
 - All Figure Page
 - Back to All Figure Page
 
                
                    
                        Fig. S8
                    
                    
                
                
            
        
        
    
        
            
            
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 Residual GFP allows for visualization of TrpA1b fated neurons in the in the cbfbw128/w128 mutant. A-H. Maximum intensity projections of TrpA1b:GFP expression from the same TG in a WT (A- D) or cbfbw128/w128 (E-H) embryo over five days. Scale bar: 20μm.  | 
    
                
                    
                        Expression Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Expression Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Antibody Labeling
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Phenotype Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Acknowledgments
                    
                    
                
                
            
        
        
    
        
            
            
                
                    
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      Full text @ PLoS Genet.