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Zusammenfassung Ablauf einer PCR

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Ablauf einer PCR (gezielte Vervielfältigung von DNA-Abschnitten)




1. Auftrennen des DNA-Doppelstranges durch Schmelzen (92°C-95°C) in
Einzelstränge durch Lösung der Wasserstoffbrückenbindungen zwischen den
komplementären Basen der DNA  Denaturierung




2. Zugabe und Anlagerung von komplementären Primern (DNA-Nucleotide)
jeweils am 3`Ende beider DNA-Einzelstränge (freie OH- Gruppe am C3-Atom
des Zuckers Desoxyribose) bei 50°C-60°C)  Hybridisierung




3. Zugabe einer hitzestabilen „Taq-Polymerase“ aus dem Bakterium thermus
aquaticus .
Synthese der beiden Tochterstränge entlang der beiden Einzelstränge (von
3`5`) bei 72°C  Synthese




Diese Reaktionsfolge wird bis zu 35-mal wiederholt, um genügend Genkopien zu
erhalten.


Document information

Study
Gymnasium
School year
2
Summarized whole book?
No
Which chapters are summarized?
Keine ahnung
Uploaded on
July 20, 2021
Number of pages
1
Written in
2020/2021
Type
Summary
$5.18

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