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Purification procedure for the isolation of a P-I metalloprotease and an acidic phospholipaseA

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Academic year: 2019

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Fig. 1 a Chromatographic profile of the crude venom of B. atrox on a Sephacryl S-200 molecular exclusion column
Fig. 2 a Chromatographic profile of fraction S3 on a DEAE Sepharose anion exchange column
Fig. 4 a Chromatographic profile of fraction 6 on a C18 reverse phase column. Elution was performed using a RP-HPLC system at a flow rate of 0.5 mL/minute using a segmented concentration gradient of 0-60 % solvent B in three column volumes, 60-80 % in five
Fig. 6 Isoelectric focusing of the toxins isolated from B. atrox venom on a 7 % polyacrylamide gel
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