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Polak J.M., Van Noorden S. — Introduction to Immunocytochemistry
Polak J.M., Van Noorden S. — Introduction to Immunocytochemistry



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Íàçâàíèå: Introduction to Immunocytochemistry

Àâòîðû: Polak J.M., Van Noorden S.

Àííîòàöèÿ:

The small size of this book is misleading. It has a wealth of theoretical and practical information. ...This book is a classic of immunhostochemistry, with the necessary information to help novices and seasoned individuals explore specific areas. The information presented is clear... This affordable book should be in every laboratory performing immunohistochemistry as well as on the bookshelf of researchers and diagnosticians who rely on this technique.


ßçûê: en

Ðóáðèêà: Õèìèÿ/

Ñòàòóñ ïðåäìåòíîãî óêàçàòåëÿ: Ãîòîâ óêàçàòåëü ñ íîìåðàìè ñòðàíèö

ed2k: ed2k stats

Èçäàíèå: 2nd

Ãîä èçäàíèÿ: 1997

Êîëè÷åñòâî ñòðàíèö: 141

Äîáàâëåíà â êàòàëîã: 12.11.2006

Îïåðàöèè: Ïîëîæèòü íà ïîëêó | Ñêîïèðîâàòü ññûëêó äëÿ ôîðóìà | Ñêîïèðîâàòü ID
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Ïðåäìåòíûé óêàçàòåëü
$\beta$-D-Galactosidase      2 27 37 39 122
$\beta$-D-Galactosidase in double immunoenzymatic stain      37 39
$\beta$-D-Galactosidase, development      122
3-Amino-9-ethylcarbazole (AEC)      25 118—119
3-Amino-9-ethylcarbazole (AEC) in multiple staining      36—39 (Plates 5 14)
4-Chloro-1-naphthol      25
4-Chloro-1-naphthol in multiple staining      119
Absorption control for specificity      133—134
Adherence of sections to slides      16 110—111
Adherence of sections to slides, poly-L-lysine      16 110—111
Adherence of sections to slides, silane (APES)      16 111
Alkaline phosphatase anti-alkaline phosphatase (APAAP)      51
Alkaline phosphatase anti-alkaline phosphatase (APAAP) in multiple staining      37 39
Alkaline phosphatase anti-alkaline phosphatase (APAAP), build-up method      63
Alkaline phosphatase in multiple staining      36—39 (Plates 12—14)
Alkaline phosphatase, blocking endogenous enzyme      26
Alkaline phosphatase, development      119—121
Alkaline phosphatase, development, blue end-product      120
Alkaline phosphatase, development, blue-brown end-product      120—121
Alkaline phosphatase, development, red end-product      36 38 120
Alkaline phosphatase, mechanism of action      26
Antibody, application to preparations      45—46
Antibody, characteristics      9—10 44—45
Antibody, characteristics, affinity      9
Antibody, characteristics, avidity      9
Antibody, characteristics, diluent      42 110
Antibody, characteristics, dilution      10 42—44
Antibody, characteristics, dilution in relation to background      36 38 8) 42—44
Antibody, characteristics, dilution in relation to sensitivity      37 39 10) 44
Antibody, characteristics, dilution in relation to temperature      43
Antibody, characteristics, dilution in relation to titration      43
Antibody, characteristics, dilution in relation to titre      10
Antibody, characteristics, IgG reaction with antigen      44—45
Antibody, monoclonal      8
Antibody, production      5—7
Antibody, production, immunization      5—6
Antibody, region-specific      6—7 61
Antibody, storage      110
Antibody, testing, blotting methods      6 93—94
Antibody, testing, ELISA      6 92—93
Antibody, testing, immunocytochemical titration      6 36 38 8) 42—44
Antibody, testing, RIA      6 92
Antigen retrieval      16—20
Antigen retrieval, enzyme pretreatment      17—18 114—115
Antigen retrieval, enzyme pretreatment, chymotrypsin      18
Antigen retrieval, enzyme pretreatment, neuraminidase      115
Antigen retrieval, enzyme pretreatment, pepsin      115
Antigen retrieval, enzyme pretreatment, protease XXTV      18 114
Antigen retrieval, enzyme pretreatment, trypsin      18 114
Antigen retrieval, heat-mediated      19—20 116—117
Antigen retrieval, heat-mediated, microwave method      36 38 116
Antigen retrieval, washing      17
Applications of immunocytochemistry      95—100
Applications of immunocytochemistry, pathological diagnosis      95—96
Applications of immunocytochemistry, quantification      97—100
Applications of immunocytochemistry, quantification, confocal microscopy      37 39 16) 98
Applications of immunocytochemistry, quantification, FACS      98 99
Applications of immunocytochemistry, quantification, flow cytometry      98—99
Applications of immunocytochemistry, quantification, supra-optimal dilution      99—100
Applications of immunocytochemistry, research      97
Avidin—biotin methods      51—54 125—128
Avidin—biotin methods, ABC versus PAP      37 39 10)
Background staining      see Non-specific staining
Biotin      2 29
Biotin in ABC methods      51—54
Biotin, blocking endogenous biotin      52—53 112
buffers      41
Buffers, PBS      41 109
Buffers, TBS      41 109
Colloidal gold, label for electron microscopical, immunocytochemistry      85—86 133—135
Colloidal gold, label for electron microscopical, multiple labelling      87—88
Colloidal gold, label for electron microscopical, quantification      97
Colloidal gold, label for electron microscopical, with Protein A or G      86
Colloidal gold, label for light microscopical, dark-field illumination      106
Colloidal gold, label for light microscopical, epipolar illumination      106
Colloidal gold, label for light microscopical, immunocytochemistry      2 20 21 27—28
Colloidal gold, label for light microscopical, labelling antibodies      21 27
Colloidal gold, label for light microscopical, silver intensification      27 128—130
Colloidal gold, label for light microscopical, uses      28
Controls      55—62 96 133—134
Controls, absorption with antigen      59 60 133—134
Controls, absorption with serum      58
Controls, absorption with tissue powder      60
Controls, experimental      61—62
Controls, negative      61 96
Controls, positive      61 96
Controls, testing for non-specific binding      55—58
Controls, testing for non-specific binding, by primary antibody      55—57
Controls, testing for non-specific binding, by second or third reagents      57
Controls, testing for non-specific binding, due to basic proteins in tissue      58
Controls, testing for unwanted specific, binding      58—60
Controls, testing for unwanted specific, due to cross-reactivity with related antigens      58—59
Controls, testing for unwanted specific, due to unknown tissue antigens      57
Counterstains to mask autofluorescence      31
Counterstains, fluorescent      21—22
Definition of immunocytochemistry      1
Detergent for permeabilization      14
Detergent to prevent non-specific binding      41 42
Diaminobenzidine (DAB)      24—25
Diaminobenzidine (DAB) for electron microscopical immunoperoxidase      84
Diaminobenzidine (DAB), intensification of reaction product      66—70
Diaminobenzidine (DAB), intensification of reaction product, cobalt      123
Diaminobenzidine (DAB), intensification of reaction product, copper sulphate      37 39 122
Diaminobenzidine (DAB), intensification of reaction product, gold chloride      123
Diaminobenzidine (DAB), intensification of reaction product, imidazole      123
Diaminobenzidine (DAB), intensification of reaction product, nickel      37 39 14) 124
Diaminobenzidine (DAB), mechanism of reaction      25
Diaminobenzidine (DAB), re-use      118
Diaminobenzidine (DAB), safety      24—25 118
Dot blots, as antibody test      94
Double immunoenzymatic staining      37 39 78 131
Double immunofluorescence staining      iv (front cover illustration) 76 77 79 105
Electron microscopical, fixation      81—82
Electron microscopical, fixation, glutaraldehyde      82
Electron microscopical, fixation, paraformaldehyde      82
Electron microscopical, immunolabelling      81—88 132—133
Electron microscopical, labels      84—86
Electron microscopical, labels, colloidal gold      85—86
Electron microscopical, labels, ferritin      84
Electron microscopical, labels, peroxidase      84—85
Electron microscopical, multiple labelling      87—88
Electron microscopical, pretreatment      87
Electron microscopical, principles      81
Electron microscopical, procedure      86 132—133
Electron microscopical, resins      82—83
ELISA, as antibody test      92—93
Endogenous enzyme blocking alkaline phosphatase      26
Endogenous enzyme blocking peroxidase      24 112—113
Endogenous enzyme blocking peroxidase, frozen sections and whole cells      113
Endogenous enzyme blocking peroxidase, paraffin sections      112—113
Enhancement of standard methods, build-up methods      63—65
Enhancement of standard methods, build-up methods, ABC      64—65
Enhancement of standard methods, build-up methods, APAAP      63
Enhancement of standard methods, build-up methods, indirect      63—64
Enhancement of standard methods, build-up methods, PAP      63—64
Enhancement of standard methods, during reaction      67 123—125
Enhancement of standard methods, intensification of, peroxidase/DAB/$H_2O_2$ product      66—70 122—124
Enhancement of standard methods, post-reaction      66—67 122—123
Enhancement of standard methods, tyramine signal amplification      67—70
Enzyme labels      2 20 23—27
Enzyme labels, $\beta$-D-galactosidase      2 27 37 39
Enzyme labels, $\beta$-D-galactosidase, development      122
Enzyme labels, alkaline phosphatase, blocking endogenous enzyme      26
Enzyme labels, alkaline phosphatase, development      119—121
Enzyme labels, alkaline phosphatase, in multiple staining      36—39 (Plates 12—14)
Enzyme labels, alkaline phosphatase, mechanism of action      26
Enzyme labels, glucose oxidase      2 26—27
Enzyme labels, glucose oxidase, development      122
Enzyme labels, peroxidase, blocking endogenous enzyme      24
Enzyme labels, peroxidase, development      24—26 66—70 117—119 122—125
fixation      11—15
Fixation for electron microscopical, immunocytochemistry      81—82
Fixation, combination      13—14
Fixation, combination, Bouin's      13
Fixation, combination, periodate-lysine-paraformalde-hyde      14
Fixation, combination, Zamboni's      13
Fixation, cross-linking      12—13
Fixation, cross-linking, formalin      12 82
Fixation, cross-linking, glutaraldehyde      12 82
Fixation, freeze-dried tissue      15
Fixation, fresh tissue      14
Fixation, pre-fixed, non-embedded tissue      14—15
Fixation, precipitant      13
Fixation, precipitant, acetone      13 14
Fixation, precipitant, alcohol      13 14
Fluorescent labels      1—2 20 21—23
Fluorescent labels, advantages      21
Fluorescent labels, AMCA      22
Fluorescent labels, counterstains      21
Fluorescent labels, disadvantages      21
Fluorescent labels, fluorescein      iv (front cover illustration) 1—2 20 22 36—39 4 15 16)
Fluorescent labels, fluorescein, labelling procedure      21—22
Fluorescent labels, microscopy      105
Fluorescent labels, mountants      106
Fluorescent labels, new fluorophores, CyDyes$^{TM}&      22
Fluorescent labels, new fluorophores, Oregon Green$^{TM}$      22
Fluorescent labels, phycoerythrin      22
Fluorescent labels, rhodamine      22
Fluorescent labels, Texas Red      iv (front cover illustation) 22
Fluorescent labels, uses      23
Glucose oxidase      2 26—27 121
Glucose oxidase, development      121
Hapten      2 29
Hapten, hapten sandwich method      29
history      1
Immunofluorescence      1—2 20 21—23 36—39 4 15 16)
Immunofluorescence in double staining      iv (front cover illustration) 76 77 79 105
Immunofluorescence, counterstains      21
Immunofluorescence, microscopy      105
Immunofluorescence, mountants      106
Immunofluorescence, quantification      97—99
Immunofluorescence, quantification, confocal microscopy      98
Immunofluorescence, quantification, FACS      98—99
Immunofluorescence, quantification, flow cytometry      98—99
Immunofluorescence, uses      23
Immunogold staining for electron microscopy      85—88 132—133
Immunogold staining for electron microscopy, double labelling      87—88
Immunogold staining for light microscopy      27 132—133
Immunogold staining for light microscopy with silver intensification      27 132—133
Immunoperoxidase staining      36 38 see
Immunostaining methods      125—133
Immunostaining methods, immunostaining, all preparations      127—128
Immunostaining methods, initial procedures      125—127
Immunostaining methods, initial procedures, fresh cryostat sections      125—126
Immunostaining methods, initial procedures, paraffin sections      125
Immunostaining methods, initial procedures, pre-fixed frozen sections      126
Immunostaining methods, initial procedures, semithin resin sections      126—127
Immunostaining methods, initial procedures, whole cell preparations      126
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, during reaction      67
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, during reaction, cobalt      67 123
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, during reaction, imidazole      67 123
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, during reaction, nickel      37 39 14) 67 124—125
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, during reaction, tyramine signal amplification      67—70
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, post-reaction      66—70
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, post-reaction, copper sulphate      37 39 66 122
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, post-reaction, gold chloride      66 123
Intensification of peroxidase/ DAB/$H_2O_2$ reaction, post-reaction, silver salts      67
Labelled probes — non- in situ hybridization of nucleic acids      101—102
Labelled probes — non-, lectin histochemistry      101
Labelled probes — non-, receptor localization      100—101
Labelled probes — non-immunocytochemical uses      100—102
labels      1—2 20—29
Labels, biotin      2 29
Labels, colloidal gold      27—28 85—86 128—130 131—133
Labels, enzyme      2 23—27
Labels, fluorescent      21—23
Labels, hapten      2 29
Labels, radioisotope      2 28—29
Methods, APAAP      51 63
Methods, automation      46—47
Methods, avidin-biotin      51—54
Methods, direct (one-step)      47—48
Methods, electron microscopical      81—88 132—133
Methods, general considerations      41—44
Methods, general considerations, antibody diluent      42
Methods, general considerations, antibody dilution      42—43
Methods, general considerations, buffers      41—42
Methods, general considerations, nature of antibodies      44—45
Methods, general considerations, reaction temperature      43—44
Methods, general considerations, reaction time      43
Methods, general considerations, sensitivity      44
Methods, immunogold with silver intensification      27 128—130
Methods, indirect (two-step)      47—49
Methods, multiple immunostaining      73—79 131
Methods, multiple immunostaining, for electron microscopical immuno-labelling      87—88
Methods, PAP      50—51
Methods, procedure for immunostaining      125—133
Microscopy      105—107
Monoclonal antibodies      8—9
Monoclonal antibodies, advantages      8
Monoclonal antibodies, control for non-specific binding      57
Monoclonal antibodies, dilution for immunocytochemistry      10
Monoclonal antibodies, disadvantages      8—9
Monoclonal antibodies, production      8
Multiple staining      73—79 131
Multiple staining, primary antibodies from different species      76—79 87—88 131
Multiple staining, primary antibodies from different species, immunoenzymatic      37 39 78 131
Multiple staining, primary antibodies from different species, immunofluorescence      iv (front cover illustration) 76 77 79 105
Multiple staining, primary antibodies from same species      73—77
Nomarski optics      106
Non-specific (background) staining      24—27 29—31 52—61
Non-specific (background) staining, antibody factors      57—59
Non-specific (background) staining, antibody factors, binding (specific) to unknown antigens      57
Non-specific (background) staining, antibody factors, binding to basic proteins      57—58
Non-specific (background) staining, antibody factors, cross-reaction (specific) with related antigens      58—59
Non-specific (background) staining, antibody factors, cross-reaction (specific) with tissue Ig      58
Non-specific (background) staining, remedies      30—31 56 60—61
Non-specific (background) staining, testing      55—58
Non-specific (background) staining, tissue factors      30—31 55—57
Non-specific (background) staining, tissue factors, autofluorescence      31
Non-specific (background) staining, tissue factors, basic proteins      58
Non-specific (background) staining, tissue factors, charged sites      30
Non-specific (background) staining, tissue factors, cross-reactivity (specific) of Ig      58
Non-specific (background) staining, tissue factors, cross-reactivity (specific) of related antigens      58—59
Non-specific (background) staining, tissue factors, endogenous biotin      52—53 112
Non-specific (background) staining, tissue factors, endogenous enzyme      23—27
Non-specific (background) staining, tissue factors, Fc receptors      30
Non-specific (background) staining, tissue factors, hydrophobic reaction      30
Peroxidase      2 24—26
Peroxidase, blocking endogenous enzyme      24 112—113
Peroxidase, development      24—26 117—119
Peroxidase, development, 3-amino-9-ethylcarbazole (AEC)      25 36—39 12) 118—119
Peroxidase, development, 4-chloro-1-naphthol      25—26 119
Peroxidase, development, diaminobenzidine      24—25 66—70 118—119 122—125
Peroxidase, development, phenol tetrazolium      26 119
Peroxidase-anti-peroxidase (PAP), method      50—51 125—128
Peroxidase-anti-peroxidase (PAP), versus ABC      37 39 10)
Photomicrography      106—107
poly-L-lysine, as absorption control      58
poly-L-lysine, as section adhesive      16 110—111
Problems and remedies      56
Quantification      97—100
Quantification, confocal microscopy      37 39 16) 98
Quantification, FACS      98—99
Quantification, flow cytometry      98—99
Quantification, supraoptimal dilution      99—100
Radioactive labels      28—29
Radioimmunoassay, as antibody test      92
Requirements for immunocytochemistry      11—13
Saving failed reactions      65—66
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