Appunti di Principi-BiolMol CTF - Capitolo3 - Omero

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• Step 4Apyrase, a nucleotide-degrading enzyme, continuouslydegrades unincorporated nucleotides and ATP. Whendegradation is complete, another nucleotide is added.
• Step 5Addition of dNTPs is performed sequentially. It should be noted thatdeoxyadenosine -thio triphosphate (dATP·S) is used as a substitutefor the natural deoxyadenosine triphosphate (dATP) since it isefficiently used by the DNA polymerase, but not recognized by theluciferase. As the process continues, the complementary DNA strandis built up and the nucleotide sequence is determined from the signalpeaks in the Pyrogram trace.
Page 3 and 4:
Impieghi della PCR• Strategie di
Page 5 and 6:
TemperaturePCR100Melting94 o C500T
Page 7 and 8:
TemperaturePCR10050Melting94 o CAnn
Page 9 and 10:
TemperaturePCR10050Melting94 o CAnn
Page 11 and 12:
Dopo n cicli il miscuglio di reazio
Page 14 and 15:
Fasi della PCR Denaturazione (melti
Page 16 and 17:
• * Si possono usare al posto del
Page 18 and 19:
Nested PCR
Page 20:
Hot Start PCR
Page 23:
Sintesi del cDNA
Page 27:
• L’elettroforesi su gel dei pr
Page 30 and 31:
IMPIEGHI DELLA PCRDiagnosi infezion
Page 33 and 34:
Test geneticoAmplificazionemediante
Page 35 and 36:
PCR-ARMS (Amplification RefractoryM
Page 37 and 38:
PCR-ARMS (Amplification RefractoryM
Page 39 and 40:
PCR-SSCP (Single Strand Conformatio
Page 41 and 42:
Page 43 and 44:
Page 45 and 46:
PCR-HAD (HeteroDuplex Analysis)•
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PCR-HAD (HeteroDuplex Analysis)
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PCR-DGGE (Denaturation Gradient Gel
Page 51 and 52:
PCR-DGGE (Denaturation Gradient Gel
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Resa della PCRResa effettiva: effet
Page 55 and 56:
Soluzioni per PCR quantitativa Util
Page 57 and 58:
Perché Real-Time?• Misura l'ampl
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Analisi tramite software
Page 61 and 62:
SYBR greenUtilizzauna molecola fluo
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SYBR green Dopo l’annealing dei p
Page 65 and 66:
SYBR green Metodica semplicePossono
Page 67: Sonde TaqMan La sonda di tipo TaqMa
Page 71 and 72: ForwardProbeReverse
Page 73 and 74: Reporter-QuencherDyeQuencher5,6 FAM
Page 75 and 76: Real-Time PCR:attività 5’>3’ e
Page 77 and 78: Real-time PCR: reagenti COMPONENTI
Page 79 and 80: 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: • Step 3ATP sulfurylase converts
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 and 132: Overview of ABI SOLiD SequencingChe
Page 133 and 134: Bead DepositionDeposit 3’ modifie
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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