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Protein Protocols Protein Protocols

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1144 Index<br />

Phenol-sulfuric acid assay, 803–804<br />

Phosphopeptides, 673–679<br />

Phosphopeptide mapping, 673–679<br />

Phosphor imaging, 222<br />

Phosphorylation (see <strong>Protein</strong><br />

phosphorylation)<br />

Photopolymerization, 116, 126–128<br />

PMSF, 1099<br />

Polyacrylamide gels (see also <strong>Protein</strong> stains<br />

and <strong>Protein</strong> blotting)<br />

electroelution, 299–304<br />

formation of, 61<br />

fractionation range of, 59, 66–67<br />

staining of proteins in, 238–239,<br />

243–248, 251–257, 259–262,<br />

233–234, 265–270, 295–297,<br />

280–290<br />

structure of, 62<br />

Polyacrylamide gel electrophoresis (see<br />

Electrophoresis)<br />

Polyclonal antibodies (see Antibodies and<br />

IgG)<br />

Polyethylene glycol, purification of IgG,<br />

991<br />

Polyvinyl alcohol, 412<br />

Ponceau S stain, 218, 390<br />

Porous graphitized carbon (PGC), 819–820,<br />

829–830<br />

Prolidase, 564<br />

Pronase,563–564<br />

Pronase E, 669<br />

Pro-Q Emerald 300 dye staining, 767–768<br />

Protease inhibitors, 1099<br />

<strong>Protein</strong> A, 406, 993<br />

<strong>Protein</strong> A mimetic, 1013–1023<br />

<strong>Protein</strong> G, 406, 410, 993<br />

<strong>Protein</strong> L, 406, 410, 993<br />

<strong>Protein</strong> LA, 405, 410, 993<br />

<strong>Protein</strong>s<br />

protein blotting, 76-77, 215–224,<br />

317–319, 321–333, 335–336,<br />

337–340<br />

acid-urea gels, 337–340<br />

blocking solutions, 218, 223, 330–332<br />

blotting (transfer) buffer, 217, 221,<br />

324–326<br />

capillary, 335–336<br />

detection by chemifluorescence,<br />

421-428<br />

detection by ECL, 218–219, 429–436<br />

detection with antibodies, 405–413<br />

detection with avidin-biotin, 415–418<br />

digestion of proteins on, 523–532, 676<br />

double relica blotting, 222<br />

electroblotting, 317–319, 337–340<br />

membranes, 327–328<br />

re-use of blots, 439–451<br />

semidry, 321–333<br />

staining of blots, 218, 273–285, 276–279,<br />

375–378, 387–391, 393–403<br />

cross-linking, 367–369<br />

DNA cross linking, 747, 753–757<br />

digestion, 511–516, 563–565<br />

kinases, 605<br />

ladder sequencing, 587, 733–738<br />

molecular weight standards, 575<br />

palmitoylation, 633–638<br />

phosphorylation, 603–608, 609–621,<br />

673–679<br />

prenylation, 641–654, 657–669<br />

quantitation of<br />

BCA assay, 11–14, 23–30<br />

Bradford method, 15–20<br />

copper iodide, 381–385<br />

flow cytometry, 45–49<br />

in gels, 231–235, 237–242<br />

kinetic silver staining, 51–54<br />

Lowry method, 7–9, 23–30<br />

nitric acid method, 31–39<br />

on blots, 429–436<br />

radiolabeled, 231–235<br />

UV absorbance, 3–6<br />

radiolabeling, 369–370, 546–547,<br />

963–964, 967–968, 969–970,<br />

971–975<br />

stains (gels and blots)<br />

Alcian blue, 773–776<br />

amido black, 390<br />

aurodye forte, 398–399<br />

auroprobe BL plus, 397–398<br />

calconcarboxylic acid, 259–262<br />

Coomassie brilliant blue, 58, 64, 67,<br />

94, 390<br />

Coomassie brilliant blue G, 238–240<br />

copper iodide, 381–385<br />

DIG-Anti-DIG AP labeling, 761–765<br />

direct blue,71<br />

Eosin Y, 295–297

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