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. 2005 Feb;79(3):1470–1479. doi: 10.1128/JVI.79.3.1470-1479.2005

FIG. 6.

FIG. 6.

Capsid protein processing products. The indicated virus samples were electrophoresed in parallel on conventional SDS-10% PAGE and SDS-16% PAGE Schagger gels. After electrophoresis, CA fragments were detected by immunoblotting with an anti-HIV-1-CA antibody which recognizes the HIV-1 CTD. Approximate fragment sizes in kilodaltons are indicated and were estimated by comparison with migration distances of known standards, assuming a linear relationship between migration and log molecular mass.