ROR2 Antibody (CL5950) [DyLight 488] Summary
                         
                                
                                
                                
            | Immunogen | This antibody was generated using a synthetic peptide of Q01974, with the exact immunogen sequence remaining proprietary. | 
            | Isotype | IgG1 | 
            | Clonality | Monoclonal | 
            | Host | Mouse | 
            | Gene | ROR2 | 
            | Purity | Protein A purified | 
            | Innovator's Reward | Test in a species/application not listed above to receive a full credit towards a future purchase. | 
                                
                          Applications/Dilutions
                                
                                    
                                    
                                        
                              
                                  | Dilutions | Immunocytochemistry/ Immunofluorescence Immunohistochemistry-Paraffin 
 | 
            | Application Notes | Optimal dilution of this antibody should be experimentally determined. | 
                                    
                                  Packaging, Storage & Formulations
            | Storage | Store at 4C in the dark. | 
            | Buffer | 50mM Sodium Borate | 
            | Preservative | 0.05% Sodium Azide | 
            | Purity | Protein A purified | 
Notes
                    
                        
DyLight (R) is a trademark of Thermo Fisher Scientific Inc. and its subsidiaries.
                     Alternate Names for ROR2 Antibody (CL5950) [DyLight 488]
                     Background
 
                    
                    ROR2 is encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors.  The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development.  Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.
                      Limitations
 
                    
                    This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are 
guaranteed for 1 year from date of receipt.
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Applications: IHC, WB
                                     
                                 
                              
                            
                                  
                                       
                                                Species: Mu
Applications: IHC, WB
                                     
                                 
                             
                            
                                  
                                       
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                                                Species: Hu, Mu, Rt
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                                                Species: Hu, Mu, Rt
Applications: ICC, WB
                                     
                                 
                              
                            
                                  
                                       Species: Hu, Mu, Rt
Applications: IHC,  IHC-P, WB
                                     
                             
                            
                                  
                                       Species: Hu
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