| Background: | The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. | 
| Applications: | ELISA, IHC | 
| Name of antibody: | FGF13 | 
| Immunogen: | Synthetic peptide of human FGF13 | 
| Full name: | fibroblast growth factor 13 | 
| Synonyms: | FGF2; FHF2; FHF-2; FGF-13 | 
| SwissProt: | Q92913 | 
| ELISA Recommended dilution: | 5000-10000 | 
| IHC positive control: | Human esophagus cancer and Human thyroid cancer | 
| IHC Recommend dilution: | 40-200 | 

		
 
	
		 
 
	
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