Figure 5. SEPT5 levels in platelet and brain lysates. (A) Protein concentrations in mouse platelet lysates samples were determined and similar protein amounts were loaded into a reducing 4% to 20% SDS-PAGE. After electrophoresis, the proteins were transferred to nitrocellulose and immunoblotted with an anti-SEPT5 monoclonal antibody (LJ-33). As previously shown, the predominant SEPT5 signal present in platelet lysates is approximately 45 kDa. Quantitation revealed a 2- to 3-fold increase in SEPT5 levels in platelets from GP IbβNull animals. (B) The same membrane was subsequently reacted with an anti-14-3-3ζ polyclonal antibody to document the approximate protein load for each lane using 14-3-3ζ (32 kDa) as an internal standard. (C) Equal quantities of brain lysates protein were analyzed by SDS-PAGE and immunoblotting for the septin protein, SEPT5. (D) The filter shown in panel C was reprobed for 14-3-3ζ protein and is shown for comparison.
Figure 5.

SEPT5 levels in platelet and brain lysates. (A) Protein concentrations in mouse platelet lysates samples were determined and similar protein amounts were loaded into a reducing 4% to 20% SDS-PAGE. After electrophoresis, the proteins were transferred to nitrocellulose and immunoblotted with an anti-SEPT5 monoclonal antibody (LJ-33). As previously shown, the predominant SEPT5 signal present in platelet lysates is approximately 45 kDa. Quantitation revealed a 2- to 3-fold increase in SEPT5 levels in platelets from GP IbβNull animals. (B) The same membrane was subsequently reacted with an anti-14-3-3ζ polyclonal antibody to document the approximate protein load for each lane using 14-3-3ζ (32 kDa) as an internal standard. (C) Equal quantities of brain lysates protein were analyzed by SDS-PAGE and immunoblotting for the septin protein, SEPT5. (D) The filter shown in panel C was reprobed for 14-3-3ζ protein and is shown for comparison.

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