Directly transforming PCR-amplified DNA fragments into plant cells is a versatile system that facilitates the transient expression assay.

PCR amplification using specific primers amplified a sin- gle 2.5 kb fragment in Brassica lines and the DNA se- quences of the fragments showed similarity to NBS-LRR domains present

The coding sequence of Escherichia coli gsiA, which encodes the ATP-binding protein of a glutathione im- porter, was amplified by PCR, and then inserted into a prokaryotic

Restriction patterns of 70 Campylobacter jejuni strains, and the reference strain, obtained using restriction endonuclease Hae III applied to PCR-amplified 702

With the aid of DDRT-PCR, we com- pared the mRNA content of cells stimulated with various cytokines or microbial products and searched for cDNA fragments that could represent genes

Testing฀for฀HCV฀antibodies฀was฀performed฀with฀a฀third฀ generation฀ enzyme฀ immunoassay฀ (EIA-3;฀ Biomeriéux฀ Co.)฀ following฀ the฀

The aim of the present study was to identify the species of Aspergillus that contaminate the inside of coffee beans collected in the stage of maturation and drying, from 16

Here we report the identification of lines ‘A’ and ‘B’ within the ‘Baia Periforme’ derived onion population, ‘Alfa São Francisco’, based on a PCR marker system

Current laboratory diagnostic methods for the identification of parasites include: polymerase chain reaction (PCR), random amplified polymorphic DNA (RAPD), amplified