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The performance of LNMO and graphite electrodes that experienced full-cell cycling for >100 cycles were then evaluated in fresh half-cells.
Cells, which were acclimatized for 30 cycles, were then tested for butanol tolerance (up to 2.25%v/v).
Two further transmission cycles were then established between successive pairs of infected and naïve, contact exposed pigs (TC3, TC4).
Twenty-five amplificycles cycles were then performed.
Five PCR cycles were then performed to amplify the reverse transcription products.
AFM force-distance cycles were then collected on a cell of interest using an antibody-functionalized cantilever with a nominal spring constant of 20 pN·nm−1.
Similar(44)
Life cycles are then clustered on the basis of estimated regression coefficients.
The MCB and essential cycles are then derived as a by-product.
Each of these cycles is then split up into s slots.
The source and magnitude of nitric oxide (NO) emissions produced by different cycles are then investigated.
The cycles are then combined in a specific way such that they become a model for an ideal absorption refrigeration cycle.
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