Examples of 'hours after transfection' in a sentence

Meaning of "hours after transfection"

hours after transfection - This phrase specifies a certain amount of time that has passed following a process called 'transfection', which is the introduction of foreign genetic material into cells. It is commonly used in scientific or biomedical research to describe experimental time frames or to discuss the effects of transfection on cellular behavior

How to use "hours after transfection" in a sentence

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hours after transfection
Forty eight hours after transfection the arteries were removed.
The cells were shocked with glycerol 8 hours after transfection.
Forty eight hours after transfection cells are harvested and assayed for CAT activity.
Cells were tested for their responsiveness to vasopressin 48 hours after transfection.
At 30 hours after transfection the cells were analysed for fluorescence in a FACSCalibur.
Serum was added 4 hours after transfection.
Minireplicon activity was increased when heat shock was performed at 2 hours after transfection.
Cells were harvested at 48 hours after transfection and luciferase activity was measured.
Toxicity was measured by determining total cellular protein in the wells 48 hours after transfection.
Cells were washed four hours after transfection with methionin-free medium.
Fresh media including the appropriate selection drugs were added 24 hours after transfection.
Forty-eight hours after transfection the cells were transferred to new plates.
Our results indicate that the virus could be recovered as early as 36 hours after transfection.
Cells were harvested 48 hours after transfection for either protein assays or RNA analysis.
Cells were fixed and stained using an antibody targeting human tyrosinase 24 hours after transfection.

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Cells were grown for 24 hours after transfection before assessment.
Cells were fixed and stained using antibodies targeting the indicated protein 48 hours after transfection.
Cells were plated 24 hours after transfection.
The cells were visually inspected under a microscope to qualitatively inspect cell death 64 hours after transfection.
Cells were assayed 48 hours after transfection.
Transfection efficiency was monitored by green fluorescent protein ( GFP ) visualization 24 hours after transfection.
Assessment was carried out 72 hours after transfection using RT-qPCR.
Total cell lysate was collected from serum starved cells with SFM for 48 hours after transfection.
Cells were harvested 48 hours after transfection for flow cytometry experiments.
Cellular uptake studies were performed 36 hours after transfection.
Cells were harvested 24 hours after transfection and scraped and pelleted.
Fluorescence was clearly detectable within 20 hours after transfection.
Cells were harvested 28 hours after transfection and CAT activity was determined.
Conditioned media were collected 60 hours after transfection.
RNA was isolated 72 hours after transfection and gene expression was quantified by RT-qPCR.
Here in both cases virus antigen was detected 24 hours after transfection using IFA.
Forty-eight hours after transfection with siRNA duplexes, the levels of endogenous EZH2 protein were quntitated.
Conditioned medium was harvested 48 hours after transfection.
At 48 hours after transfection a scratch was made with 20 µl pipette tip.
Luciferase activity was measured 48 hours after transfection.
Twelve hours after transfection the cells were grown in medium containing 0.2 % serum for 24 hours.
The cells were lysed 48 hours after transfection.
Twenty four hours after transfection the eukaryocidal antibiotic puromycin ( 1.1 µg / ml ) was added to the cultures.
The supernatant were harvested 96 hours after transfection.
About 5-6 hours after transfection with siRNA 's, the cells were infected with PRRSV.
The cells were collected 72 hours after transfection.
Generally, the treatments, collection and lysis of the cells occurred 48 hours after transfection.
FVIII activity was measured 48 hours after transfection by one-stage clot assay.
In two of three experiments, virus was first detected at 24 hours after transfection.
Cells were glycerol shocked 12 hours after transfection and collected after 72 hours by ATV.
The luciferase activities were measured 48 hours after transfection.
Cell viability was determined at 96 hours after transfection by CellTiter-Glo luminescent assay from Promega.
Cells were harvested and extracts prepared 48 hours after transfection.
Supernatant media were sampled 65 hours after transfection and assayed for p24 Gag protein expression levels.
The cells were imaged with confocal 24 hours after transfection.

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