background: parasitic nematodes cause animal and human diseases of major socio-economic importance worldwide. the suppression of parasite development at particular developmental stages could provide an alternative approach for nema-tode control. in this study, ascaris suum was used as a model system in the study of the differentially expressed genes in the infective l3 stage. methods: the gene ...

objectives: in present study we aimed to clone the lux i gene encoding n-acyl-homoserine synthase detected in biofilm forming clinical isolates of acinetobacter baumannii and study its expression in escherichia coli transformants. materials and methods: four a. baumannii hospital strains which demonstrated strong biofilm activity were selected in this investigation. the presence of lux i gene w...

introduction: the estrogen receptors are potential candidates in prognosis and particularly in predicting hormone response therapy in breast cancer. the aim of this study was to measure erα gene expression due to study of the association between erα expression, age and menopause of iranian women with breast cancer. methods: 21 adenocarcinoma cases with grade 2 and 10 normal samples were screene...

Unlike classical end-point analysis PCR, real-time PCR provides the data required for quantification of the target nucleic acid. The results can be expressed in absolute terms by reference to external quantified standards or in relative terms compared to another target sequence present within the sample. Absolute quantification requires that the efficiency of the amplification reaction is the s...

We have developed a novel "real time" quantitative PCR method. The method measures PCR product accumulation through a dual-labeled fluorogenic probe (i.e., TaqMan Probe). This method provides very accurate and reproducible quantitation of gene copies. Unlike other quantitative PCR methods, real-time PCR does not require post-PCR sample handling, preventing potential PCR product carry-over conta...

Those who have worked in the field of quantitative polymerase chain reaction (PCR) since the early 1990s have accepted many of the tedious aspects of the early assays as routine. Difficulties associated with early quantitative PCR techniques included: (i) ensuring that the PCR was within the linear range of amplification (that portion where the PCR signal is directly proportional to the input c...