368
SUBJECT INDEX
Bacteriological technique, 42-43, 192, 265,
299, 323, 326, 329
Barium permanganate stain, 240
Basement membranes, staining, 236, 245
(Fig. 29)
Beam
damage, 50, 82, 125, 307 (Figs. 9, 25)
flicker,
289, 296-297
intensity, 269, 288, 293, 307-308, 309,
320
Bennett and Luft's collidine buffered tetroxide, 40-41
Benzoyl peroxide, catalyst, 97-98, 119-120,
121, 124
Benzyldimethylamine,
accelerator,
110,
115
Bibliographies, 357
Block
hardness, 92-95, 163
mounting, 133-135, 355 (Fig. 13)
orientation, 131-135, 173-174 (Fig. 13)
serial sections for, 212
size, 95, 105, 130, 163, 177, 181, 182,
186, 310, 355
staining, 236, 239, 241
trimming,
129-134,
173-174,
182,
355
(Fig. 13)
wetting, 92, 93, 126, 174-175, 187
Botanical techniques, 37, 50, 63, 65, 340
Buffers
cacodylate, 53, 55, 57
collidine, 40
dichromate, 41-42
Michaelis (see Veronal buffer)
phosphate, 39-40, 50-52, 55, 57
Veronal, 36, 38-39, 42-44, 56, 63-65
Butylhydroperoxide, catalyst, 119
Butylmethacrylate, 97, 103, 121, 124, 136
Butyl perbenzoate, initiator, 118
C
Cacodylate buffer, 53, 55
Cadmium iodide stain, 348
Calibration, 214, 361
Cambridge ultramicrotome, 144-145
Capsules, embedding, 86, 87, 89, 113, 355
Carbon evaporation (see
vacuum
evaporation)
Carbon films (see supporting films)
Carbon replicas, 327, 335-336, 339, 341
Carbon-14, radioisotope, 251
Cardolite NC 513,
flexibilizer-hardener,
113, 115
Caulfield's
isotonic
osmium
tetroxide,
37-38
Cellulose acetate replicas, 344
Chatter, 94, 130, 170, 173, 178, 180-182,
186, 310 (Fig. 21)
Chromatic aberration, 281
Chromium for shadowing, 332-333 (Figs.
9, 41)
Chromotrope, 261
Chromyl chloride stain, 75, 242-243
Circuit instability, 280, 294-298, 309
Claude's acidic osmium tetroxide, 44
Cleaning glassware, 91
Cleaved surfaces, 326
Clevenger's ultramicrotome, 147-148
Cobalt naphthenate, activator, 118
Cold stage, 307
Collagen, 193, 206, 236, 244, 328, 354 (Fig.
29)
Collidine buffer, 40
Column alignment, 280-282
Compensation (see objective lens)
Condenser aperture
alignment, 288
contamination, 297
sources, 362
use, 269
Condenser lens
alignment, 282, 284, 285, 287-288
double, 269, 282, 293
Congresses, International, 357-358
Conjugated antibody stains, 247-250
Connective tissue sectioning, 163, 173
Contamination (see also specified by position as lens, aperture, section, stain,
etc.)
bombardment damage, 306-307
glass knives, 177, 182-184, 186
lead stains, 221, 225, 227-229 (Fig. 10)
phosphotungstic acid stain, 237
SUBJECT INDEX
Bacteriological technique, 42-43, 192, 265,
299, 323, 326, 329
Barium permanganate stain, 240
Basement membranes, staining, 236, 245
(Fig. 29)
Beam
damage, 50, 82, 125, 307 (Figs. 9, 25)
flicker,
289, 296-297
intensity, 269, 288, 293, 307-308, 309,
320
Bennett and Luft's collidine buffered tetroxide, 40-41
Benzoyl peroxide, catalyst, 97-98, 119-120,
121, 124
Benzyldimethylamine,
accelerator,
110,
115
Bibliographies, 357
Block
hardness, 92-95, 163
mounting, 133-135, 355 (Fig. 13)
orientation, 131-135, 173-174 (Fig. 13)
serial sections for, 212
size, 95, 105, 130, 163, 177, 181, 182,
186, 310, 355
staining, 236, 239, 241
trimming,
129-134,
173-174,
182,
355
(Fig. 13)
wetting, 92, 93, 126, 174-175, 187
Botanical techniques, 37, 50, 63, 65, 340
Buffers
cacodylate, 53, 55, 57
collidine, 40
dichromate, 41-42
Michaelis (see Veronal buffer)
phosphate, 39-40, 50-52, 55, 57
Veronal, 36, 38-39, 42-44, 56, 63-65
Butylhydroperoxide, catalyst, 119
Butylmethacrylate, 97, 103, 121, 124, 136
Butyl perbenzoate, initiator, 118
C
Cacodylate buffer, 53, 55
Cadmium iodide stain, 348
Calibration, 214, 361
Cambridge ultramicrotome, 144-145
Capsules, embedding, 86, 87, 89, 113, 355
Carbon evaporation (see
vacuum
evaporation)
Carbon films (see supporting films)
Carbon replicas, 327, 335-336, 339, 341
Carbon-14, radioisotope, 251
Cardolite NC 513,
flexibilizer-hardener,
113, 115
Caulfield's
isotonic
osmium
tetroxide,
37-38
Cellulose acetate replicas, 344
Chatter, 94, 130, 170, 173, 178, 180-182,
186, 310 (Fig. 21)
Chromatic aberration, 281
Chromium for shadowing, 332-333 (Figs.
9, 41)
Chromotrope, 261
Chromyl chloride stain, 75, 242-243
Circuit instability, 280, 294-298, 309
Claude's acidic osmium tetroxide, 44
Cleaning glassware, 91
Cleaved surfaces, 326
Clevenger's ultramicrotome, 147-148
Cobalt naphthenate, activator, 118
Cold stage, 307
Collagen, 193, 206, 236, 244, 328, 354 (Fig.
29)
Collidine buffer, 40
Column alignment, 280-282
Compensation (see objective lens)
Condenser aperture
alignment, 288
contamination, 297
sources, 362
use, 269
Condenser lens
alignment, 282, 284, 285, 287-288
double, 269, 282, 293
Congresses, International, 357-358
Conjugated antibody stains, 247-250
Connective tissue sectioning, 163, 173
Contamination (see also specified by position as lens, aperture, section, stain,
etc.)
bombardment damage, 306-307
glass knives, 177, 182-184, 186
lead stains, 221, 225, 227-229 (Fig. 10)
phosphotungstic acid stain, 237