Design of endonuclease restriction sites into primers for PCR cloning.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 12490457.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
I present a software system PCRCLNG that facilitates the design of endonuclease restriction sites into the 5'-end of PCR primers. The product amplified using these primers can be directly cloned into vectors. The program estimates the annealing temperature for each primer and selects the primer pairs with comparable annealing temperature. Finally the software determines whether the PCR product can be cloned into the vector to generate in-frame gene fusion.
Medical subject headings
- Cloning, Molecular
- DNA Primers
- DNA Restriction Enzymes
- Polymerase Chain Reaction
- Software