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Exact(14)
5 µl of RNase A were then added (1 mg/ml) to the supernatant and incubated at 55°C for one hour.
Lysostaphin and RNase A were then added to concentrations of 50 µg ml−1 and 60 µg ml−1, respectively, and the mixture was incubated at 37°C for 30 minutes.
The 2 tracts generated (A to B and B to A) were then overlaid, thresholded, and binarized.
The indicated concentrations of β-tan and Sal A were then prepared in complete EMEM (10% FBS), with 5 nM TPA and placed over the solidified cell agar layer.
Tubes from the series of source plates (A) were then transferred to the destination series of plates (B) according to the designed scheme.
The values of a were then correlated with the P-δ data by the time elapsed since the beginning of each test.
Similar(46)
The mutant A is then introduced at low frequency.
The expression vectors pCM13 SELP-1020-A), pCM13 SELP-1020-A, pCM13 SELP-520-A and pCM13 SELP-520-A) were then transformed to E. coli BL21(DE3) for pCM13 SELP-59-Aion.
A is then also a non-valid sentence of MFC.
For a = ρx, a is then a 1D peak.
Juguloarterial (j-a) gradients were then calculated.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com