Polymerase chain reaction (PCR) is a very powerful tool for qualitative evaluation of nucleic acids due to its high efficiency and convenience. Together with the reverse transcription (RT) reaction, the PCR method has been widely applied to the quantitative measurement of DNA and RNA messages. Since RT-PCR is much more sensitive than all of the traditional methods for quantification of mRNA, in...

I n the last few years, molecular hybridization methods have been used extensively in basic and applied virology because of their technical flexibility and high specificity. Using these techniques, the detection of DNA and RNA viruses directly from clinical specimens, the analysis of the specific transcriptional activity of viral genes in vitro and in vivo, and the study of virus-host relations...

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 ...

Something I notice often in supervising new graduate students is their frustration with the irreproducibility of their biological data. For example, I am asked frequently ‘‘how many biological replicates do I need for qRT-PCR’’? The answer, of course, lies first with the students themselves. They need as many replicates as will persuade them of the validity of their observations. However, for m...

background: hox genes are well-known transcription factors that play essential roles in directing embryonic development. tgifly is a y-linked homeobox gene that was originally identified by virtue of its expression in adult testis. the functions of tgifly in normal and abnormal development are unknown. methods: to investigate the potential roles of tgifly gene in the infertile males, a semi-nes...

BACKGROUND This study was to investigate some new pathological genes in colorectal adenocarcinoma of human. METHODS Human colorectal adenocarcinoma tissues and normal colorectal tissues were taken and suppression subtractive hybridization (SSH) and cDNA microarray techniques were employed. From differentially expressed 86 expressed sequence tags (EST), 10 EST of the SSH were selected as seed ...