Sentence examples for sample cells and from inspiring English sources

The suggested system accommodates up to 24 sample cells with a field of view of 35 mm or 12 sample cells and 12 calibration cells for a seamless replacement of the optodes to follow processes that last longer than the optode lifetime.

Each sample (cells and supernatants) was collected from the well and cells were lysed by freezing and thawing (−80°C to 37°C) three times.

The system thereby creates a working channel in order to be able to administrate or sample cells and substances to/from the extra-vasal space, and to make closure of the vessel wall safe.

Newly designed sample cell and N2 mixing technique provided higher elemental sensitivity with smoother signal intensity profiles.

This method uses a sample cell and an in-situ FTIR to obtain the time profiles of dynamic interactions of adsorbing species on NP samples.

The heating body is closely coupled with the sample cell, and there is a hole on the side wall of the furnace for the entrance of the microlens.

A solution (0.25 mmol/L) of ArgRS was placed in the sample cell, and a 2.5 mmol/L solution of Arginine was added in a series of 20 injections, the heat evolved was recorded at 25°C.

This concept was tested with a benchtop spectrophotometer equipped with a 1- and 10-cm path length sample cell and modified with linear polarizers to measure the birefringence of suspended particles.

Competition experiments were performed by placing equimolar amounts of TCL1A and IκB_ank7CS in the sample cell, and injecting AKT_PH.

For the IkBα TCL1A titration, IκB_ank7CS (45 µM) was kept in the sample cell, and TCL1A (470 µM) was injected.

After equilibration at 35°C, the reaction was started by injecting mitochondria into the sample cell, and the heat change was recorded for 20 min. The volume of mitochondria suspension injected in the sample cell varied between 15 and 45 µl, and the mitochondrial protein concentration in the calorimeter cell varied between 10 and 30 µg/ml.