Polymerase chain reaction (PCR)
GPTKB entity
Statements (45)
Predicate | Object |
---|---|
gptkbp:instance_of |
gptkb:Biology
|
gptkbp:application |
gptkb:forensic_science
gptkb:research genetic testing medical diagnostics cloning gene expression analysis pathogen detection |
gptkbp:average_temperature |
typically 50-65° C for annealing
typically 72° C for extension typically 94-98° C for denaturation |
gptkbp:developed_by |
gptkb:Kary_Mullis
|
gptkbp:first_introduced |
gptkb:1983
|
gptkbp:has_limitations |
contamination risk
requires specific primers not suitable for all DNA types |
https://www.w3.org/2000/01/rdf-schema#label |
Polymerase chain reaction (PCR)
|
gptkbp:improves |
real-time PCR
fast PCR techniques high-fidelity polymerases isothermal amplification |
gptkbp:involves |
thermal cycling
|
gptkbp:products |
PCR products
DNA copies amplified DNA fragments |
gptkbp:protocol |
gptkb:cooperative
annealing denaturation |
gptkbp:related_to |
gptkb:gene_therapy
gptkb:biotechnology DNA sequencing molecular diagnostics genomics |
gptkbp:requires |
gptkb:RNA_Polymerase
nucleotides DNA template primers |
gptkbp:type_of |
multiplex PCR
digital PCR nested PCR quantitative PCR (q PCR) reverse transcription PCR (RT-PCR) |
gptkbp:used_for |
amplifying DNA
|
gptkbp:bfsParent |
gptkb:Kary_B._Mullis
|
gptkbp:bfsLayer |
5
|