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						Background: 
					 
						The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia. Two transcript variants encoding different isoforms have been found for this gene. 
					 
						Applications: 
					 
						ELISA, WB 
					 
						Name of antibody: 
					 
						PTPN11 
					 
						Immunogen: 
					 
						Fusion protein of human PTPN11 
					 
						Full name: 
					 
						protein tyrosine phosphatase, non-receptor type 11 
					 
						Synonyms: 
					 
						CFC, NS1, SHP2, BPTP3, PTP2C, PTP-1D, SH-PTP2, SH-PTP3 
					 
						SwissProt: 
					 
						Q06124 
					 
						ELISA Recommended dilution: 
					 
						1000-5000 
					 
						WB Predicted band size: 
					 
						68 kDa 
					 
						WB Positive control: 
					 
						NIH/3T3 cells 
					 
						WB Recommended dilution: 
					 
						200-1000 
					
		
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
			
					 
				
					 
			
				 
		
	
					 
				
					 
			
 
	
 
	