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   An alternative method to isolate protease and phospholipase A2 toxins from snake venoms based on partitioning of aqueous two-phase systems  
   
نویسنده gómez g.n. ,nerli b.b. ,acosta o.c. ,picó g.a. ,leiva l.c.a.
منبع journal of venomous animals and toxins including tropical diseases - 2012 - دوره : 18 - شماره : 3 - صفحه:306 -316
چکیده    Snake venoms are rich sources of active proteins that have been employed in the diagnosis and treatment of health disorders and antivenom therapy. developing countries demand fast economical downstream processes for the purification of this biomolecule type without requiring sophisticated equipment. we developed an alternative,simple and easy to scale-up method,able to purify simultaneously protease and phospholipase a2 toxins from bothrops alternatus venom. it comprises a multiple-step partition procedure with polyethylene-glycol/phosphate aqueous two-phase systems followed by a gel filtration chromatographic step. two single bands in sds-polyacrylamide gel electrophoresis and increased proteolytic and phospholipase a2 specific activities evidence the homogeneity of the isolated proteins. © cevap 2012.
کلیدواژه Isolation; Partition; Proteases; Snake toxins
آدرس protein research laboratory (labinpro),biochemistry department,school of natural and exact sciences,northeast national university (unne),(3400) corrientes, Argentina, lab of physical chemistry app. to bioseparation processes,dept. of physical chemistry,school of biochemical and pharmaceutical sciences,national university of rosario,rosario, Argentina, school of veterinary science,northeast national university (unne),corrientes, Argentina, lab of physical chemistry app. to bioseparation processes,dept. of physical chemistry,school of biochemical and pharmaceutical sciences,national university of rosario,rosario, Argentina, protein research laboratory (labinpro),biochemistry department,school of natural and exact sciences,northeast national university (unne),(3400) corrientes, Argentina
 
     
   
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