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Cytotoxicity of nanostructures was determined by MTT cell proliferation assay [12], a quantitative, convenient method to evaluate a cell population's response to external factors.
This study was designed to evaluate a cell proliferation marker, including the percentage of cycling cells (MIB1), and the duration of the cell cycle (assessed by argyrophilic nucleolar organizer regions proteins [AgNORs] measurement).
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Validating and evaluating a cell counting measurement process can be difficult because of the lack of appropriate reference material.
The objective is to develop and evaluate a PVA cell immobilization technology in degrading diesel in seawater.
To address this hypothesis, we evaluated Ad association with cells in both unsynchronized and pharmacologically synchronized cell populations.
In this study, we used a parasite engineered to express green fluorescent protein (GFP) to evaluate a single-cell sorting method for rapidly cloning Plasmodium falciparum.
Flow cytometry can efficiently evaluate a number of cells at the single-cell level in a short time and isolate a single clone from sub-populations.
Here, we evaluate an eukaryotic cell-free translation system based on the WGE (wheat germ embryo) [ 24] for the expression of a highly toxic AahII scorpion venom protein.
We present and evaluate a new approach to cell immobilization for use in cell-based biosensors.
The proliferation rate of both populations was evaluated using a cell DNA assay.
The number of cells per milliliter in the prepared suspension was evaluated using a cell counter (Coulter-Z, Beckman Coulter, Inc., Indianapolis, IN, USA).
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