Ãëàâíàÿ    Ex Libris    Êíèãè    Æóðíàëû    Ñòàòüè    Ñåðèè    Êàòàëîã    Wanted    Çàãðóçêà    ÕóäËèò    Ñïðàâêà    Ïîèñê ïî èíäåêñàì    Ïîèñê    Ôîðóì   
blank
Àâòîðèçàöèÿ

       
blank
Ïîèñê ïî óêàçàòåëÿì

blank
blank
blank
Êðàñîòà
blank
Bagasra O., Hansen J. — In Situ PCR Techniques
Bagasra O., Hansen J. — In Situ PCR Techniques



Îáñóäèòå êíèãó íà íàó÷íîì ôîðóìå



Íàøëè îïå÷àòêó?
Âûäåëèòå åå ìûøêîé è íàæìèòå Ctrl+Enter


Íàçâàíèå: In Situ PCR Techniques

Àâòîðû: Bagasra O., Hansen J.

Àííîòàöèÿ:

This book describes comprehensive step-by-step protocols for the delineation of genetic amplification and histological detection techniques. Each procedure has been tested and validated for its sensitivity, precision, and reproducibility, and the authors give advice on the design of primers for PCR applications and on optimizing these protocols for use with plant, insect, and prokaryotic cells.


ßçûê: en

Ðóáðèêà: Òåõíîëîãèÿ/

Ñòàòóñ ïðåäìåòíîãî óêàçàòåëÿ: Ãîòîâ óêàçàòåëü ñ íîìåðàìè ñòðàíèö

ed2k: ed2k stats

Ãîä èçäàíèÿ: 1997

Êîëè÷åñòâî ñòðàíèö: 160

Äîáàâëåíà â êàòàëîã: 12.11.2006

Îïåðàöèè: Ïîëîæèòü íà ïîëêó | Ñêîïèðîâàòü ññûëêó äëÿ ôîðóìà | Ñêîïèðîâàòü ID
blank
Ïðåäìåòíûé óêàçàòåëü
Acetate buffer solution      99
AES silane, glass slide preparation      30—31
Ampli-Taq Gold, in situ PCR, hot start technique      57—58
Amplicon length, primer design      13
Amplicons: in situ PCR amplification, immunohistochemistry applications      63
Amplicons: sequencing and cloning      64—66
Amplification procedures: amplicon recovery for sequencing and cloning      64—66
Amplification procedures: chromosomal applications      68—72
Amplification procedures: conventional sealing technologies      49—51
Amplification procedures: conventional sealing technologies, Self-Seal      51—53
Amplification procedures: cover glass attachment with nail polish      54—55
Amplification procedures: electron microscopy      61—62
Amplification procedures: gene therapy regimes      66—68
Amplification procedures: hot start technique      56—58
Amplification procedures: immunohistochemistry      62—63
Amplification procedures: in situ PCR      49—60
Amplification procedures: multiple signals, multiple labels in individual cells      64
Amplification procedures: one-step reverse transcription      53—54
Amplification procedures: optimization with Self-Seal technology      51—53
Amplification procedures: plant tissues      73—75
Amplification procedures: protocols      49—54
Amplification procedures: rare event detection      119—125
Amplification procedures: sealing and tissue attachment alternatives      55—56
Amplification procedures: solutions for      98—99
Amplification procedures: thermal cyclers      58—60
AMVRT (Avian myeloblastosis virus reverse transcriptase) enzyme: in situ PCR      46—47
AMVRT (Avian myeloblastosis virus reverse transcriptase) enzyme: primers for      49
AMVRT (Avian myeloblastosis virus reverse transcriptase) enzyme: temperature calculations      16
Annealing: chain reaction      4
Annealing: DNA primer design      10
Annealing: in situ PCR, hot start technique      56—58
Annealing: solution-based PCR      24
Annealing: temperature calculations      16—18
Annealing: touchdown protocols for primers and probes      16—18
Archival tissue, preparation      36
Bone fragments, DNA in      22
Bone marrow cells, amplification techniques      120—123
CD34 cells, in situ PCR techniques, gene therapy regimes      67—68
cDNA: in situ PCR: heat-stabilization treatment      38
cDNA: in situ PCR: primers for RT reaction      48—49
cDNA: in situ PCR: reverse transcriptase      8—9
cDNA: RNA target primer design      11—12
cDNA: solution-based RNA PCR      25—26
Cell cultures: in situ PCR techniques, chromosome spreads      70—71
Cell cultures: on glass slides      32
Cell surface antigens, in situ PCR amplification      63
Cell suspensions: DNA/RNA extraction      20—21
Cell suspensions: tissue preparation      31
Cellular antigens, in situ PCR amplification      63
Chain reaction mechanism      3—7
Chain reaction mechanism, annealing      4
Chain reaction mechanism, denaturation      4
Chain reaction mechanism, extension temperature      5
Chain reaction mechanism, geometric amplification      6—7
Chain reaction mechanism, oligonucleotide primers      3—4
Chain reaction mechanism, thermal cycle      5—6
Chitin resistance, plant tissue in situ PCR      71—72
Chromosome amplification: in situ PCR techniques      68—72
Chromosome amplification: in situ PCR techniques, cell arrest at mitotic metaphase      71
Chromosome amplification: in situ PCR techniques, harvesting      71—72
Chromosome amplification: in situ PCR techniques, slide preparation      72
Chromosome amplification: in situ PCR techniques, spread protocols      69—70
Chromosome amplification: solutions for      99
Cloning, in situ PCR amplification, amplicon recovery      64—66
Color solution, formula for      99
Commercial primers, availability      12—13
Computer-assisted design (CAD), primer design      109—118
Control procedures, in situ polymerase chain reaction (PCR)      93—95
Coplin jars      97
Cover glasses, in situ PCR, nail polish attachment of      54—55
Degenerate primers, chain reaction      4
Denaturation, chain reaction      4
Deoxyribonucleoside triphosphates (dNTPs), polymerase chain reaction (PCR) mechanism      3
Detection systems, solution-based PCR and      26—28
DNA fingerprinting, polymerase chain reaction (PCR) development      2
DNA polymerase: polymerase chain reaction (PCR) mechanism      3
DNA polymerase: reverse transcriptase and      8—9
DNA: amplification, primer-probe designs      15—16
DNA: commercial extraction preparations      20
DNA: extraction protocols      20—22
DNA: in bone fragments or forensic material      22
DNA: in paraffin-embedded tissue      21—22
DNA: in situ PCR: heat-stabilization treatment      37—38
DNA: in situ PCR: multiple signals and individual cell labeling      64
DNA: in situ PCR: proteinase K digestion      40
DNA: in situ PCR: sealing protocols      49
DNA: reverse transcription      7—9
DNA: solution-based PCR and      23—24
DNA: target primer design      9—10
DNAase: DNA Engine      58
Dot blot testing, solution-based PCR probes and detection systems      26—28
Downstream (antisense) primer: in situ PCR, reverse transcriptase reaction      46—47
Downstream (antisense) primer: in situ PCR, RNA target primer design      10—12
Downstream (antisense) primer: in situ PCR, RNA targets      44—45
Downstream (antisense) primer: in situ PCR, RNAase-free, DNAase solution      45—46
Downstream (antisense) primer: in situ PCR, RT reactions      48—49
Downstream (antisense) primer: in situ PCR, treatment protocols      45—47
Downstream (antisense) primer: reverse transcription      13
Downstream (antisense) primer: solution-based RNA PCR      25—26
Electron microscopy, in situ PCR amplification      62—63
Enzyme digestion, plant tissue in situ PCR      74—75
Ethanol, paraffin-fixed tissue slides      32—33
Extension temperature, polymerase chain reaction (PCR)      5
Ficoll — Hypaque density gradient, cell suspension tissue preparation      31
Fixation techniques, in situ PCR      38—39
Forensic material, DNA in      22
Formalin fixation: archival tissue preparation      36
Formalin fixation: in situ PCR amplification, cellular antigens      63
Frame Seal gaskets, in situ PCR techniques      56—58
Frozen sections, preparation techniques      33—36
FTTC labeling, in situ PCR amplification, immunohistochemistry      62—63
Gel electrophoresis, solution-based PCR      24—25
GenBank: oligonucleotide primers      3—4
GenBank: sequence data      14—15
GenBank: sequence retrieval      109—111
Gene Cone sealing technology: amplicon recovery      66
Gene Cone sealing technology: in situ PCR techniques      55—56
Gene therapy, in situ PCR techniques      66—68
GeneReleaser      20
Geometric amplification, polymerase chain reaction (PCR)      6—7
Glass slides: AES silanation      30—31
Glass slides: cell cultures      32
Glass slides: in situ PCR, chromosome spreads      72
Glass slides: plant tissue in situ PCR      75
Glass slides: sealing technologies      29—30
Glass slides: sources      96—97
Glass staining dishes      97
Harvesting techniques, in situ PCR, chromosome spreads      71—72
Heat-stabilization treatment, in situ PCR      37—38
HLA typing, polymerase chain reaction (PCR) development      2
HLA-DQa genes, in situ PCR, validation and control procedures      94—95
Hot start technique, in situ PCR      56—58
Human immunodeficiency virus-1 (HIV-1), in situ PCR analysis: automated microscopic detection      125
Human immunodeficiency virus-1 (HIV-1), in situ PCR analysis: chromosome spreads      68—69
Human immunodeficiency virus-1 (HIV-1), in situ PCR analysis: gene therapy regimes      67—68
Human immunodeficiency virus-1 (HIV-1), in situ PCR analysis: rare event detection      124—125
Human immunodeficiency virus-1 (HIV-1), in situ PCR analysis: validation and control procedures      93—95
Human immunodeficiency virus-1 (HIV-1), in situ PCR analysis: viral burden quantitation      125
Hydrogen peroxide, PBS solution and      98
Immunocytochemistry (ICC), rare event detection      119
Immunohistochemical techniques: frozen tissue preparation      34
Immunohistochemical techniques: in situ PCR amplification      62—63
In situ hybridization (ISH): automated microscopic HIV-1 detection      125
In situ hybridization (ISH): buffer solution      99
In situ hybridization (ISH): comparison with other techniques      78—79
In situ hybridization (ISH): directly incorporated labeled nucleotides, posthybridization      92
In situ hybridization (ISH): empirical characteristics      79—80
In situ hybridization (ISH): in situ PCR protocols      80—84 86—92
In situ hybridization (ISH): in situ PCR protocols, alkaline-phosphatase color posthybridization      90—92
In situ hybridization (ISH): in situ PCR protocols, detection methods      83
In situ hybridization (ISH): in situ PCR protocols, digoxigenin-labeled probe posthybridization      92
In situ hybridization (ISH): in situ PCR protocols, FITC posthybridization      88—89
In situ hybridization (ISH): in situ PCR protocols, general hybridization      86—87
In situ hybridization (ISH): in situ PCR protocols, hybridization controls      83—84
In situ hybridization (ISH): in situ PCR protocols, labeling      82—83
In situ hybridization (ISH): in situ PCR protocols, probe characteristics      80—81
In situ hybridization (ISH): in situ PCR protocols, synthetic oligo probe      81—82
In situ hybridization (ISH): in situ PCR protocols, time, temperature and concentration      82
In situ hybridization (ISH): oligonucleotide probe labeling      84—86
In situ hybridization (ISH): peroxidase-based color posthybridization      89—90
In situ hybridization (ISH): peroxidase-based color posthybridization, $^{33}P$ probe posthybridization      88
In situ hybridization (ISH): radioactive probes vs. nonradioactive detection      79
In situ hybridization (ISH): rare event detection      119—120
In situ hybridization (ISH): sealing and attachment alternatives      55—56
In situ hybridization (ISH): Self-Seal technology      51—53
In situ hybridization (ISH): thermal cyclers      58—60
In situ hybridization (ISH): validation and controls      93—95
In situ polymerase chain reaction (PCR): amplicon recovery for sequencing and cloning      64—66
In situ polymerase chain reaction (PCR): amplification procedures      49—60
In situ polymerase chain reaction (PCR): chromosomal applications      68—72
In situ polymerase chain reaction (PCR): cover glass attachment with nail polish      54—55
In situ polymerase chain reaction (PCR): digestion optimization      43—44
In situ polymerase chain reaction (PCR): DNAase treatment: reverse transcriptase reaction      46—47
In situ polymerase chain reaction (PCR): DNAase treatment: RNA targets      44—45
In situ polymerase chain reaction (PCR): DNAase treatment: RNAase-free DNAase solutions      45—46
In situ polymerase chain reaction (PCR): electron microscopy      61—62
In situ polymerase chain reaction (PCR): gene therapy regimes      66—68
In situ polymerase chain reaction (PCR): hot start technique      56—58
In situ polymerase chain reaction (PCR): immunohistochemistry      62—63
In situ polymerase chain reaction (PCR): multiple signals, multiple labels in individual cells      64
In situ polymerase chain reaction (PCR): nonradioactive-labeled nucleotides      60
In situ polymerase chain reaction (PCR): one-step reverse transcription      53—54
In situ polymerase chain reaction (PCR): plant tissues      73—75
In situ polymerase chain reaction (PCR): protocols      37—43 49—50
In situ polymerase chain reaction (PCR): protocols, fixation and washes      38—39
In situ polymerase chain reaction (PCR): protocols, heat-stabilization treatment for DNA/RNA messages      37—38
In situ polymerase chain reaction (PCR): protocols, proteinase K treatment      39—43
In situ polymerase chain reaction (PCR): rare event detection      123—125
In situ polymerase chain reaction (PCR): reaction primers      48—49
In situ polymerase chain reaction (PCR): RT enzymes      47—48
In situ polymerase chain reaction (PCR): schematic overview      48
In situ reactions, annealing temperature calculations      17—18
Infectious disease, rare event detection      123—125
Liquid nitrogen, frozen tissue preparation      35
Methyl celluloacetate ether (MCA), plastic sections tissue preparation      33
Methyl methacrylate (MMA), plastic sections tissue preparation      33
MMLVRT (Moloney murine leukemia virus reverse transcriptase) enzyme in situ PCR      46—47
MMLVRT (Moloney murine leukemia virus reverse transcriptase) enzyme in situ PCR, primers for      49
Monoclonal antibodies, in situ PCR, hot start technique      57—58
Mononuclear cells, DNA/RNA extraction      20—21
mRNA: in situ PCR: amplification, multiple signals and individual cell labeling      64
mRNA: in situ PCR: heat-stabilization treatment      38
mRNA: in situ PCR: primers for RT reaction      48—49
mRNA: in situ PCR: proteinase Ê digestion      40
mRNA: RNA target primer design      11—12
mRNA: solution-based RNA PCR      25—26
Nail polish sealing technique      29—30
Nail polish sealing technique, in situ PCR: amplicon recovery      66
Nail polish sealing technique, in situ PCR: conventional protocols      50—51
Nail polish sealing technique, in situ PCR: cover glass attachment with      54—55
Nail polish, in situ PCR techniques, amplicon recovery      66
Nonradioactive nucleotides, in situ PCR      60
Nucleotides: DNA primer design      9—10
Nucleotides: in situ PCR      60
Nunc glass slides      32
Oligo d(T) primer: amplicon length      13
Oligo d(T) primer: in situ PCR: RT reaction      48—49
Oligo d(T) primer: in situ PCR: sequencing and cloning      64—66
Oligo d(T) primer: RNA target primer design      11
Oligo d(T) primer: solution-based RNA PCR      25—26
Oligo software      14
Oligonucleotide primers: chain reaction mechanism      3—4
Oligonucleotide primers: denaturation and annealing      4
Oligonucleotide primers: polymerase chain reaction (PCR) development      2
Oligonucleotides      See also Primer design
Oncology research, amplification techniques      119—125
One-step reverse transcription, in situ PCR      53—54
Paraffin-fixed tissue      32—33
Paraffin-fixed tissue, DNA extraction      21—22
Paraffin-fixed tissue, frozen sections      33—34
Paraformaldehyde, 2% solution      97
PBS solution: 0.3% hydrogen peroxide      98
PBS solution: 10x solution, pH 7.2-7.4      97
PBS solution: 1x PBS      97
PBS solution: in situ PCR      38—39
Peripheral blood monocytes (PBMCs): DNA/RNA extraction      20—21
Peripheral blood monocytes (PBMCs): in situ PCR techniques chromosome spreads      70
Peripheral blood monocytes (PBMCs): in situ PCR techniques chromosome spreads, validation and control procedures      94—95
Permiofix: frozen tissue preparation      34
Permiofix: in situ PCR amplification, immunohistochemistry      63
Phytohemagglutinin (PHA), in situ PCR techniques, chromosome spreads      69
Plant tissue, in situ PCR      73—75
Plant tissue, protoplast protocol      74—75
Plastic sections tissue preparation      33
Polymerase chain reaction (PCR): annealing temperatures      16—18
Polymerase chain reaction (PCR): chain reaction mechanism      3—7
Polymerase chain reaction (PCR): chain reaction mechanism, denaturation and annealing      4
Polymerase chain reaction (PCR): chain reaction mechanism, extension      5
Polymerase chain reaction (PCR): chain reaction mechanism, geometric amplification      6—7
Polymerase chain reaction (PCR): chain reaction mechanism, oligonucleotide primers      3—4
Polymerase chain reaction (PCR): chain reaction mechanism,second thermal cycle      5—6
Polymerase chain reaction (PCR): historical background      1—2
Polymerase chain reaction (PCR): primer design      9—16
Polymerase chain reaction (PCR): primer design, amplicon length      13
Polymerase chain reaction (PCR): primer design, commercial available primer pairs      12—13
Polymerase chain reaction (PCR): primer design, DNA targets      9—10
Polymerase chain reaction (PCR): primer design, primer-probe design      15—16
Polymerase chain reaction (PCR): primer design, RNA targets      10—12
Polymerase chain reaction (PCR): primer design, sequence data sources      14—15
Polymerase chain reaction (PCR): reverse transcription      7—9
Polymerase chain reaction (PCR): touchdown protocols      16—18
Primer design: annealing temperature calculations      16—18
Primer design: computer-assisted design (CAD)      109—118
Primer design: in situ PCR, RT reactions      48—49
Primer design: optimization      117—118
Primer design: polymerase chain reaction (PCR)      9—16
Primer design: polymerase chain reaction (PCR), amplicon length      13
Primer design: polymerase chain reaction (PCR), DNA targets      9—10
Primer design: polymerase chain reaction (PCR), primer pairs, commercial availability      12—13
Primer design: polymerase chain reaction (PCR), primer-probe design      15—16
Primer design: polymerase chain reaction (PCR), RNA targets      10—12
Primer design: polymerase chain reaction (PCR), sequence data sources      14—15
Primer dimers, DNA primer design      10
Probe design: DNA amplification      15—16
Probe design: verification of      26—28
Probe design: verification of, dot blot testing      26—28
Probe design: verification of, Southern blot testing      28
Proteinase K, solution formula      98
Proteinase K: in situ PCR      39—40
Proteinase K: in situ PCR, alternative technique      40—43
Proteinase K: in situ PCR, amplicon recovery      65—66
Proteinase K: in situ PCR,optimization of      43
Proteinase K: solution formula      98
Proteins, in situ PCR amplification, multiple signals and individual cell labeling      64
Protoplasts, in situ PCR      74—75
Random primer, RNA target primer design      11
Rare event detection: amplification techniques      119—125
Rare event detection: infectious disease      123—125
Reagents: archival tissue preparation      36
Reagents: basic formulas      97—99
Reagents: DNA/RNA extraction, commercial preparations      20
Retroviruses, reverse transcriptase in      8
Reverse transcriptase (RT) enzymes      See also specific RT enzymes
Reverse transcriptase (RT) enzymes in retroviruses      8
Reverse transcriptase (RT) enzymes in situ PCR      46—47
Reverse transcriptase (RT) enzymes in situ PCR, automated microscopic HIV-1 detection      125
Reverse transcriptase (RT) enzymes in situ PCR, primers for RT reactions      48—49
Reverse transcriptase (RT) enzymes in situ PCR, properties      47—48
Reverse transcriptase (RT) enzymes in situ PCR, rare event detection      119—125
Reverse transcriptase (RT) enzymes in situ PCR, validation and control procedures      95
1 2
blank
Ðåêëàìà
blank
blank
HR
@Mail.ru
       © Ýëåêòðîííàÿ áèáëèîòåêà ïîïå÷èòåëüñêîãî ñîâåòà ìåõìàòà ÌÃÓ, 2004-2024
Ýëåêòðîííàÿ áèáëèîòåêà ìåõìàòà ÌÃÓ | Valid HTML 4.01! | Valid CSS! Î ïðîåêòå