Skip to main content
. 1999 Feb;119(2):409–416. doi: 10.1104/pp.119.2.409

Table I.

Quantification of immunogold labeling of rice roots with the single-affinity-purified anti-NADH-GOGAT IgG

Cellular Compartment Root Tissue Type
Epidermis/Exodermis Cortex Central Cylinder
gold particles μm−2
Plastid 155.7  ± 60.21 (13) 158.0  ± 96.92  (9) 141.2  ± 37.47 (13)
Mitochondrion 108.8   (2) N.D.a 49.94  ± 12.99 (12)
Cell wall 23.94  ± 10.28   (4) 12.54  ± 3.350  (5) 12.90  ± 6.569   (6)
Cytosol 9.301  ± 4.810   (4) 16.16  ± 4.801  (6) 12.76  ± 5.395 (10)
Vacuole 0.7990  ± 0.5049 (4) 0.3562  ± 0.0767 (4) 1.260  ± 0.6878  (6)
Air space N.D. 0.3148  ± 0.4100 (4)  10.34       (2)

Rice seedlings were grown for 24 h with 1 mm NH4+. Six to nine micrographs of each of the three tissue types (epidermis and exodermis, cortex, and central cylinder) were taken from sections of root tip (<10 mm) incubated with single-affinity-purified anti-NADH-GOGAT IgG as the primary antibody, and analyzed as described in Methods. Values represent the mean ± sd immunolabeling density. Numbers in parentheses are n values.

a

N.D., Not detected.