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. 1999 Jan 19;96(2):412–417. doi: 10.1073/pnas.96.2.412

Table 1.

Quantification of immunogold-labeling of αi on plasma membranes

Sample* Number of micrographs Gold particles per group Gold particles per μm2
Control 19 3.4  ±  0.4 50 ± 7.1
GDPβS 22 4.7  ±  0.5 61 ± 8.1
GTPγS 24 8.7  ±  0.9 87 ± 7.1
*

Samples are plasma membranes torn from the upper surface of MA104 cells. Controls were fixed immediately, whereas GDPβS and GTPγS samples were incubated with 10 μM nucleotide at 37°C for 30 min before fixation and processing for immunogold labeling with affinity-purified B087 antibodies. 

Micrographs were from three independent experiments; each included all three samples. 

Gold particles were grouped on stained structures of variable shape and size (largest dimension, 20–600 nm) on the inner surface of plasma membranes; see ref. 4