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This step was repeated every 3 to 4 mm to ensure ideal tear stabilization.
Relatively large cores were selected at the tumour-advancing front (1 mm) to ensure that adequate amounts of both tumour and adjacent stroma were present for scoring.
In addition, the cutterhead life decreases nearly 45.2% with the initial crack depth increasing from 0.5 mm to 2 mm, and it is inferred that the value of initial crack depth should be controlled below 1.6 mm, to ensure the service life.
Samples were collected after mixing, and then air dried, crushed, and sieved (< 0.5 mm) to ensure homogeneity.
Again, the surgical guide should have an anterior-posterior length of about 4 6 mm to ensure stability.
An outer diameter of less than 5 mm to ensure that a significant number of the sensors remain intact after passing through the injection pumps.
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Embryos were then washed 3× in ice cold 1XPBS (10×PBS: 580 mM Na2HPO4, 170 mM NaH2PO4H2O, 680 mM NaCl) to ensure all maternal tissues were removed.
Unless stated otherwise the respiratory substrate was a mixture of GMS (5 mM L-glutamate+2 mM L-malate+5 mM succinate) to ensure electron entry at both complex I and complex II of the respiratory chain as occurs in vivo.
The results indicate that, the external and internal diameter of the annual area on the pick should be 40.6 mm and 40 mm, respectively to ensure normal shutdown of the self-controlling hydro-pick at a jet pressure 40 MPa.
In four experiments, hearts were perfused with buffer containing 1 mM palmitate, then 0.2 mM palmitate to ensure that the order of buffer change did not affect the results.
N supply increased from 3 mM N at the start of the experiment to a final concentration of 30 mM N to ensure that plants were well supplied with N. Other nutrients were supplied as 5 mM K2SO4, 2 mM MgSO4, 2 mM CaSO4, 0.457 mM KH2PO4, 42.5 µM K2HPO4, 100 µM FeEDTA, 20 µM MnSO4, 10 µM H3BO3, 1 µM CuSO4, 2.5 µM ZnSO4, 0.35 µM Na2MoO4 with tap water supplied on alternate days.
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