Article
Use of inosine-containing oligonucleotide primers for enzymatic amplification of different alleles of the gene coding for heat-stable toxin type I of enterotoxigenic Escherichia coli.
Applied and environmental microbiology - 1 Apr 1991
Candrian U, Furrer B, Höfelein C, Lüthy J
Abstract excerpt
A method which employs the polymerase chain reaction (PCR) to identify Escherichia coli strains containing the estA gene was developed. This gene codes for heat-stable enterotoxin type I. The use of an inosine-containing pair of amplification primers allowed the amplification of a specific 175-bp DNA fragment from several different estA alleles. The amplified fragments were identified and distinguished by...
Topics
- Alleles
- Animals
- Bacterial Toxins
- Base Sequence
- DNA Restriction Enzymes
- DNA, Bacterial
- Electrophoresis, Agar Gel
- Enterotoxins
- Enzyme-Linked Immunosorbent Assay
- Escherichia coli
