* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project
Download Recombinant DNA Technology
Gel electrophoresis wikipedia , lookup
DNA barcoding wikipedia , lookup
Eukaryotic transcription wikipedia , lookup
Gene expression wikipedia , lookup
Comparative genomic hybridization wikipedia , lookup
Promoter (genetics) wikipedia , lookup
Transcriptional regulation wikipedia , lookup
Maurice Wilkins wikipedia , lookup
Silencer (genetics) wikipedia , lookup
DNA sequencing wikipedia , lookup
Agarose gel electrophoresis wikipedia , lookup
Molecular evolution wikipedia , lookup
SNP genotyping wikipedia , lookup
DNA vaccination wikipedia , lookup
Real-time polymerase chain reaction wikipedia , lookup
Gel electrophoresis of nucleic acids wikipedia , lookup
Transformation (genetics) wikipedia , lookup
Non-coding DNA wikipedia , lookup
Bisulfite sequencing wikipedia , lookup
DNA supercoil wikipedia , lookup
Vectors in gene therapy wikipedia , lookup
Molecular cloning wikipedia , lookup
Community fingerprinting wikipedia , lookup
Genomic library wikipedia , lookup
Cre-Lox recombination wikipedia , lookup
Nucleic acid analogue wikipedia , lookup
Polymerase Chain Reaction ⢠Based on DNA polymerase, the enzyme that replicates DNA. â Needs template DNA and two primers that flank the region to be amplified. Primers are short (generally 18-30 bases) DNA oligonucleotides complementary to the ends of the region being amplified. â Starting at each primer, DNA polymerase adds new bases to the 3' ends to create the new second strand. â PCR is a cyclical process. Each cycle doubles the number of DNA molecules between the primers: exponential growth. â A key element in PCR is a special form of DNA polymerase from Thermus aquaticus, a bacterium that lives in nearly boiling water in the Yellowstone National Park hot springs. This enzyme, Taq polymerase, can withstand the temperature cycle of PCR, which would kill DNA polymerase from E. coli. ⢠advantages: â rapid, sensitive, lots of useful variations, robust (works even with partly degraded DNA) ⢠disadvantages: â Only short regions (up to 2 kbp) can be amplified. â limited amount of product made