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Index 1141<br />

Electrophoresis<br />

of antibodies, 1005–1007<br />

acetic acid urea gels, 103–111<br />

acid-urea triton gels, 113–122<br />

of carbohydrates, 851–858, 898–899<br />

CAT gel electrophoresis, 87–100<br />

detergents for, 134–135<br />

diagonal, 589–593<br />

2D PAGE, 131–139, 141–157, 159–162,<br />

163–168, 169–180, 181–183,<br />

185–196<br />

difference gel electrophoresis, 185–196<br />

gradient SDS PAGE, 69–72, 166<br />

isoelectric focusing, 125–129<br />

low pH, 623–626<br />

non-denaturing PAGE, 57–60<br />

non-equilibrium pH gel electrophoresis,<br />

181–183<br />

peptides, 73–79, 548–550, 553–557,<br />

599–601, 676–679<br />

SDS PAGE, 61–67, 69–72, 73–79<br />

sodium decyl sulfate PAGE, 81–86<br />

use of urea, 134–135<br />

ELISA, 1083–1088<br />

Ellman’s reagent, 483–484, 595–596<br />

Endoglycosidase H, 827<br />

Endoproteinase Glu-C, 513–516, 524–528<br />

Endoproteinase Lys-C, 524–528, 611<br />

Enhanced chemiluminescence (see ECL)<br />

Enzymatic digestion of proteins, 511–521,<br />

523–532, 563–565<br />

Enzyme linked immunosorbent assay (see<br />

ELISA)<br />

Eosin Y stain, 295–297<br />

Ethoxyformylation, 473–474<br />

Eukaryotic cells<br />

lysis of, 1102–1104<br />

radiolabeling of, 159–162<br />

Excoglycosidases, 835, 868, 875–878<br />

F<br />

Fab, 1070<br />

F(ab1 ) 2, 1069–1070<br />

Farmer’s reducer, 267<br />

Ferrozine, ferrous stain, 277, 281<br />

Flicker, 197–218<br />

Flow cytometry for protein quantitation,<br />

45–49<br />

Fluorescein isothiocyanate, 352–354<br />

Fluorochrome labeling, 351–354<br />

Fluorography, 307–312, 627<br />

FPLC, 573<br />

Free radical catalysis, 61<br />

G<br />

β-Galactosidase labeling, 345–346<br />

Gas chromatography, analysis of<br />

monosaccharides, 809–810, 811–812<br />

GC (see Gas chromatography)<br />

Gel electrophoresis (see Electrophoresis)<br />

Gel filtration (permeation) chromatography,<br />

573–578, 995–997<br />

Glutaraldehyde coupling, 958<br />

Glycoproteins<br />

analysis by mass spectrometry, 908–910<br />

characterization by lectin-binding,<br />

795–801, 844–845,917–928<br />

detection in gels and blots, 761–772,<br />

773–776, 779–791<br />

linkages, 780, 784–785, 938<br />

monosaccharide analysis, 768, 805–806,<br />

809–810, 811–812<br />

oligosaccharide release, 817–818,<br />

823–825, 827–828<br />

periodate oxiation of, 803–804<br />

phenol sulfuric acid assay, 803–804<br />

staining, 295–297, 773–776<br />

Gradient SDS PAGE, 69–72, 166<br />

H<br />

Haptens, 953<br />

HAT medium, 1111<br />

Heparan sulfatesaccharides, 893–902<br />

High pH anion exchange chromatography<br />

(see HPAEC)<br />

Histidine, ethoxyformylation of, 473–474<br />

Histones<br />

blotting of, 337–340<br />

electrophoresis of, 103–111, 113–122<br />

Horseradish peroxidase–avidin/streptavidin<br />

conjugates, 417<br />

Horseradish peroxidase–labeled antibodies,<br />

409, 445<br />

Horseradish peroxidase labeling, 347–348<br />

HPAEC analysis of monosaccharides,<br />

768–769, 805–807, 815–816,<br />

831–832, 833–838<br />

HPLC

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