PubMed Health⌕ Search

Biomedical subjects

S Mangru

Publications and source records attributed to S Mangru.

2 recordsLinked to original sources

Dynamic DNA hybridization on a chip using paramagnetic beads.

Dynamic DNA hybridization is presented as an approach to perform gene expression analysis. The method is advantageous because of its dynamic supplies of both DNA samples and probes. The approach was demonstrated on a microfluidic platform by incorporating paramagnetic beads as a transportable solid support. A glass chip was fabricated to allow simultaneous interrogation of eight DNA target samples by DNA probes. DNA targets were immobilized on beads via streptavidin-biotin conjugation or base pairing between oligonucleotide residues. The DNA/bead complex was introduced into the device in which hybridization took place with a complementary probe. The hybridized probe was then removed by heat denaturation to allow the DNA sample to be interrogated again by another probe with a different sequence of interest. A pneumatic pumping apparatus was constructed to transport DNA probes and other reagents into the microfluidic device while hydrostatic pumping was used for the introduction of paramagnetic beads with samples. After investigating three types of paramagnetic beads, we found Dynabeads Oligo(dT)25 best suited this application. Targets on the beads could be sequentially interrogated by probes for 12 times, and the hybridization signal was maintained within experimental variation. Demonstration of specific hybridization reactions in an array format was achieved using four synthesized DNA targets in duplicate and five probes in sequence, indicating the potential application of this approach to gene expression analysis.

Actins↗

Evaluation of methods for the laboratory diagnosis of malaria in Guyana.

When 297 blood samples taken from patients attending a fever clinic in Georgetown Public Hospital were examined microscopically, after thick and thin blood films had been stained with Giemsa, one hundred and forty-two (47.8%) were microscopically positive for malaria. After processing the patient's serum, samples by the Indirect Fluorescent Antibody (IFA) technique, specific IgG and IgM antibodies were detected in 239 (81.3%) and 179 (60.1%), respectively, of the sera. Based on the microscopical findings, the IFAT gave positive predictive and negative values of 54.4% and 81.8% (IgG), and 57.5% and 67.8% (IgM), suggesting that the IgM would be more useful than the IgG in the diagnosis of current malaria. An odds ratio analysis showed that the presence of symptoms, IgG or IgM antibodies, as well as visits to endemic regions, could be good indicators of current malaria. Age and occupation were not. The microscopical method will continue to be the gold standard-the best available criterion for the validation of our tests-for diagnosis of acute malaria.

Animals↗