中文名称:兔抗GBA多克隆抗体 
		
 
	
		
 
	
		
 
	
		
 
	
		
 
	
		
 
	
		
 
	
		
 
	
		
 
	
技术规格
| Background: | This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants. | 
| Applications: | ELISA, WB | 
| Name of antibody: | GBA | 
| Immunogen: | Synthetic peptide of human GBA | 
| Full name: | glucosylceramidase beta | 
| Synonyms: | GCB; GBA1; GLUC | 
| SwissProt: | P04062 | 
| ELISA Recommended dilution: | 5000-10000 | 
| WB Predicted band size: | 60 kDa | 
| WB Positive control: | Mouse heart tissue, Mouse liver tissue, Mouse brain tissue lysates | 
| WB Recommended dilution: | 500-2000 | 

	
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