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. 1998 Jul;9(7):1773–1786. doi: 10.1091/mbc.9.7.1773

Table 1.

Localization of AMF-R in HeLa and NIH-3T3 cells by immunoelectron microscopy

Smooth tubules and vesicles Rough ER Flat plasma membrane Caveolae Clathrin-coated pits and vesicles
HeLa
 AMF-R
  Gold particles (n) 660 34 147 52 3
  Membrane (μm) 328.5 187.5 245.6 14.6 19.3
  Gold particles/μm 2.01 ± 0.15 0.18 ± 0.04 0.60 ± 0.08 3.56 ± 0.53 0.16 ± 0.13
 Control
  Gold particles (n) 83 6 25 3 1
  Membrane (μm) 307.5 95.2 211.0 16.1 5.0
  Gold particles/μm 0.27 ± 0.08 0.06 ± 0.03 0.12 ± 0.05 0.19 ± 0.10 0.20 ± 0.21
NIH-3T3
 AMF-R
  Gold particles (n) 640 74 296 44 2
  Membrane (μm) 432.6 308.9 308.8 28.8 34.7
  Gold particles/μm 1.48 ± 0.10 0.24 ± 0.06 0.96 ± 0.10 1.53 ± 0.30 0.06 ± 0.06
 Control
  Gold particles (n) 33 7 10 4 2
  Membrane (μm) 303.1 109.8 138.1 31.7 6.2
  Gold particles/μm 0.11 ± 0.02 0.06 ± 0.03 0.07 ± 0.03 0.13 ± 0.06 0.32 ± 0.18

Gold particles associated with the indicated membrane organelles were counted and the density per μm membrane length determined. Control labeling was determined using a nonimmune rat IgM antibody (Benlimame et al., 1995).