Examples of using Ethidium in English and their translations into Portuguese
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Colloquial
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Official
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Medicine
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Financial
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Ecclesiastic
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Ecclesiastic
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Computer
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Official/political
Further, ethidium homodimer enters damaged membranes of the dead cells
During the experiments, the scientists observed that the molecule may help ethidium oligonucleotides(short fragments of a single strand of DNA or RNA)
Biocompatibility by gold coverage was determined by mtt assay and ethidium bromide and acridine orange staining. the results showed that the gold coverage was effective in stabilizing the sensor and degr.
Changes in cell physiology were observed by using ethidium bromide(be), bis-oxonol(box) and propidium iodide pi.
Fluorimetric studies, using ethidium bromide as probe, showed that dna is the probable cellular target.
stained with ethidium bromide on UV transilluminator.
VWR® Blue light transilluminators are often used as an alternative to UV transilluminators when users wish to use'safe dyes' instead of ethidium bromide.
While the quantification of the extracted dna was done by the nanodrop¿nd-1000 thermo scientific machine. postpone, a second quantification was realized with agarose gel at 0,8% flushed with ethidium bromide.
The induction of apoptosis was screened with the morphologic assay stained with acridine orange and ethidium bromide and with dna fragmentation assay by agarose gel electrophoresis.
the gel can be stained using colored dyes such as Coomassie Brilliant Blue or ethidium bromide to make the separated proteins appear as distinct colored bands on the gel.
USA in 0.8% agarose gel, stained with ethidium bromide 0.5 mg•mL.
Agar supplemented with ethidium bromide as well as by detection of msrA gene.
iii cell staining with fluorescein diacetate and ethidium bromide.
apoptosis were evaluated by acridine orange/ethidium bromide and hoechst 33342,
Identification of gene amplification was done using an ethidium bromide stained 1.7% agarose gel, in which 7µl of each nested PCR product was separated by electrophoresis;
were stained with 5 µmol/L ethidium homodimer and 5 µmol/L calcein-AM and incubated at 37 °C for 30 min.
by fragment size of(rflp), analyzed on 3% agarose gels stained with ethidium.
viability was analyzed by staining with calcein am and ethidium homodimer-1; proliferation was analyzed by immunolabeling with¿-ki67 antibody and trophic factor production was analyzed by immunolabeling with¿-fgf-2 antibody.
containing ethidium bromide, in the concentration of 0.5mg/mL,
1% agarose gel electrophoresis, had ethidium bromate added 5 mg/ml and sample buffer bromophenol blue 6x.