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Two optimised formulations (OF1 and OF2), for protein content and technological performance, were experimentally validated.
Model parameter identification methodology based on two optimised cyclic tests is explained and applied in the temperature range from room temperature up to 600 °C on a 55NiCrMoV7 tool steel with four different initial hardness levels.
The calibration (Hosmer-Lemeshow test) and discriminating validity (area under the ROC curve, sensitivity, specificity, likelihood ratios, predictive values) of the two optimised versions of the PSS will be evaluated.
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At the concrete level, the impact of three optimised paste mixtures on SCC properties was assessed.
PIXEL calculations were then carried out on all three optimised structures, referred to as 'opt', 'and and 'C' respectively.
So far, only three optimised BN analogues, DOTA-8-AOC-BN(7 14 NH2, AMBA DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2 DO3A-CH2CO-8-aminooctanoyl-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2
Microsatellites were amplified in seven optimised multiplex PCR as described above.
This model was employed to predict four "optimised" HLA-Cw*0102-binding HLA-Cw*0102-binding HLA-Cw*0102-bindingfinity of binding to HLA-Cw*0102.
Three optimised qRT-PCR assays revealed poor sensitivity and enabled detection of at least 10 copies/ µL.
Of the five one-step kits tested using the Mx3005P cycler, three optimised one-step kits (i.e., Quantitect-1 step, Rotor Gene-1 step, and SSIII Platinium-1 step) revealed good sensitivity with the detection of at least 10 copies/ µL.
Two fully optimised, validated, and MIQE compliant HHV-8 assays have been established with excellent sensitivity, specificity and dynamics.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com