Figure 1.
Figure 1. Western blot. After transfer to the membrane the blot was probed with anti-IVAPLA2 (Santa Cruz Biotechnology) at a 1:300 dilution and peroxidase-conjugated rabbit antimouse at the same dilution. Color development used diaminobenzidine tetra hydrochloride (DAB). Lane 1 shows molecular weight markers; lane 2, U937 cell lysate prior to Prosep column application (3 μg); lane 3, eluate from the Prosep column after U937 application (10 μg); lane 4, SDS elution from U937 Prosep column (7 μg); lane 5, SDS elution from red cell Prosep column (12 μg); lane 6, molecular weight markers; lane 7, platelet preparation (10 μg); lane 8, leukocyte preparation (39 μg). The numbers given in parentheses for each lane refers to the total protein applied to the gel.

Western blot. After transfer to the membrane the blot was probed with anti-IVAPLA2 (Santa Cruz Biotechnology) at a 1:300 dilution and peroxidase-conjugated rabbit antimouse at the same dilution. Color development used diaminobenzidine tetra hydrochloride (DAB). Lane 1 shows molecular weight markers; lane 2, U937 cell lysate prior to Prosep column application (3 μg); lane 3, eluate from the Prosep column after U937 application (10 μg); lane 4, SDS elution from U937 Prosep column (7 μg); lane 5, SDS elution from red cell Prosep column (12 μg); lane 6, molecular weight markers; lane 7, platelet preparation (10 μg); lane 8, leukocyte preparation (39 μg). The numbers given in parentheses for each lane refers to the total protein applied to the gel.

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