IFN-gamma R2 Antibody [DyLight 755] Summary
                         
                                
                                
                                
            | Immunogen | Mouse myeloma cell line NS0-derived recombinant human IFN-gamma  R2Ala22-Gln247
 Accession # P38484
 | 
            | Specificity | Detects human IFN-gamma  R2 in direct ELISAs and Western blots. | 
            | Isotype | IgG | 
            | Clonality | Polyclonal | 
            | Host | Goat | 
            | Gene | IFNGR2 | 
            | Purity | Antigen Affinity-purified | 
            | Innovator's Reward | Test in a species/application not listed above to receive a full credit towards a future purchase. | 
                                
                          Applications/Dilutions
                                
                                    
                                    
                                        
                              
                                  | Dilutions | CyTOF-ready Flow Cytometry Neutralization Western Blot 
 | 
            | 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 | Antigen Affinity-purified | 
Notes
                    
                        
DyLight (R) is a trademark of Thermo Fisher Scientific Inc. and its subsidiaries.
                     Alternate Names for IFN-gamma R2 Antibody [DyLight 755]
                     Background
 
                    
                    IFN gamma Receptor beta encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance.
                      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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