Appunti di Principi-BiolMol CTF - Capitolo3 - Omero

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Emulsion PCR/Bead EnrichmentPrepare clonal bead populations in microreactors containingtemplate, PCR reaction components, beads, and primers.After PCR, denature the templates and perform bead enrichment toseparate beads with extended templates from undesired beads. Thetemplate on the selected beads undergoes a 3’ modification toallow covalent attachment to the slide.
Bead DepositionDeposit 3’ modified beads onto a glass slide. During beadloading, deposition chambers enable you to segment a slide intoone, four, or eight sections. A key advantage of the system is theability to accommodate increasing densities of beads per slide,resulting in a higher level of throughput from the same system.
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Impieghi della PCR• Strategie di
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TemperaturePCR100Melting94 o C500T
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TemperaturePCR10050Melting94 o CAnn
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TemperaturePCR10050Melting94 o CAnn
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Dopo n cicli il miscuglio di reazio
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Fasi della PCR Denaturazione (melti
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• * Si possono usare al posto del
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Nested PCR
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Hot Start PCR
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Sintesi del cDNA
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• L’elettroforesi su gel dei pr
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IMPIEGHI DELLA PCRDiagnosi infezion
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Test geneticoAmplificazionemediante
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PCR-ARMS (Amplification RefractoryM
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PCR-ARMS (Amplification RefractoryM
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PCR-SSCP (Single Strand Conformatio
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PCR-HAD (HeteroDuplex Analysis)•
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PCR-HAD (HeteroDuplex Analysis)
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PCR-DGGE (Denaturation Gradient Gel
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PCR-DGGE (Denaturation Gradient Gel
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Resa della PCRResa effettiva: effet
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Soluzioni per PCR quantitativa Util
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Perché Real-Time?• Misura l'ampl
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Analisi tramite software
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SYBR greenUtilizzauna molecola fluo
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SYBR green Dopo l’annealing dei p
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SYBR green Metodica semplicePossono
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Sonde TaqMan La sonda di tipo TaqMa
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ForwardProbeReverse
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Reporter-QuencherDyeQuencher5,6 FAM
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Real-Time PCR:attività 5’>3’ e
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Real-time PCR: reagenti COMPONENTI
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Curve di amplificazioneFluorescenza
Page 81 and 82: QuantificazioneASSOLUTA i campioni
Page 83 and 84: Quantificazione relativaPlot di amp
Page 85 and 86: Sonde FRET(FluorescenceResonanceEne
Page 87 and 88: Molecular Beacons Durante lo step d
Page 89 and 90: Probes : ScorpionsStep 1Lo Scorpion
Page 91 and 92: Step 3Probes : ScorpionsRaffreddand
Page 93 and 94: Real-Time PCR: applicazioni‣ Quan
Page 95 and 96: Analisi della sequenzanucleotidica
Page 97 and 98: ddNTP
Page 99 and 100: • Si suddivide quindi la miscela
Page 101 and 102: ddCTPddCTPddCTPPRIMERDNA Polimerasi
Page 103 and 104: • Le diverse catene polinucleotid
Page 105 and 106: Metodo di sequenziamentodel DNA “
Page 107 and 108: Sequenziamento automatizzato con ma
Page 109 and 110: Le emissioni fluorescenti vengono c
Page 111 and 112: Metodo di Sequenziamento di Maxame
Page 113 and 114: Un altro metodo per la determinazio
Page 115 and 116: • Step 1A sequencing primer is hy
Page 117 and 118: • Step 3ATP sulfurylase converts
Page 119: • Step 5Addition of dNTPs is perf
Page 123 and 124: What is Next-Generation Sequencing?
Page 125 and 126: Illumina sequencing technology• L
Page 127 and 128: Illumina:Sequencing-bysynthesis
Page 129 and 130: Illumina sequencing technology• S
Page 131: Overview of ABI SOLiD SequencingChe
Page 136 and 137: SOLiD TechnologyLigation-basedchemi
Page 138 and 139: Exact Call ChemistryUp to 99.99% ac
Page 140 and 141: Latest Platforms:Illumina HiSeq:•
Page 142: Campi di applicazione delle piattaf
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Appunti di Principi-BiolMol CTF - Capitolo3 - Omero

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