The phrase "aspirate out" is not commonly used in written English and may not be widely understood.
It could be used in a medical or technical context, referring to the act of removing fluid or air from a body cavity or space.
Example: "The doctor decided to aspirate out the excess fluid from the patient's knee joint to relieve pressure."
Alternatives: "suction out" or "extract".
Suction was then reapplied and the water was allowed to aspirate again, until a point at which either the modeled stomach was empty or fluid ceased to aspirate out (and remained ceased for 5 min), suggesting a recurrent blockage.
The water was allowed to aspirate until a point at which either the stomach was empty or fluid ceased to aspirate out (and remained ceased for 5 min), suggesting a blockage.
Suction was applied to the NGT at -40 mm Hg, and the water was allowed to aspirate until a point at which either the model stomach was empty or fluid ceased to aspirate out (and remained ceased for 5 min), suggesting a blockage.
The hospital said that a blood clot had been "aspirated out to establish good flow in coronary arteries".
DMSO (100 μL) was added in each well after aspirating out the supernatant and incubated at 37 °C for 1 h.
After 24 h, supernatants were aspirated out and the cell monolayers in the wells were washed with 200 μL PBS (0.1 M, pH 7.4).
Supernatants from the wells were aspirated out and fresh aliquots of growth medium (containing NPs, i.e., GEM-PLGA NPs, blank PLGA NPs, GEM-Ab-PLGA NPs, and blank Ab-PLGA NPs) in desired concentrations in the range of 2 32 μg/mL were added.
After overnight growth, supernatants from the culture plates were aspirated out and fresh aliquots of growth medium containing suspension of FITC-loaded PLGA NPs and FITC-loaded Ab-PLGA NPs were added at the concentration of 0.25 mg/ml and incubated at 37 °C for 6 h.
Cells were infected in duplicates with serial 10-fold dilutions of cell culture supernatants, and incubated at 37°C for 1 hr, with gentle rocking every 15 min. After that the inoculum was aspirated out, cells were then overlaid with 2 ml of DMEM containing 10% FBS, 1% antibiotics and 1% methyl cellulose agar (Sigma).
The OVD was completely aspirated out with the rock and roll technique.
The white layer representing PBMCs was gently aspirated out and aseptically transferred into sterile centrifuge tubes.
