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The morphologies were recorded by transmission electron and field emission scanning electron microscopy analysis and these showed the formation of a few layer rGO sheets.
However, deviations from expected morphologies were recorded, and this information was used to identify vectors that partially complemented the mutant phenotype (see below).
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Growth rate and culture morphology were recorded every 3 5 days.
Changes in weight, molecular weight and morphology were recorded during hydrolysis experiments.
Growth rates and gross morphology were recorded during expansion.
Their numbers and morphology were recorded and tabulated in Table 1.
No homozygous fish with hybrid morphology were recorded, while the DFA of morphometric results suggest that most of hybrids are F1 (Fig. 1).
Changes in colony morphology were recorded at 100× magnification using an Olympus IX71 inverted microscope and Image-Pro Plus Version 5.0 software.
Three species of Nematodirus, identified initially by egg morphology, were recorded in this survey, namely N. filicollis, N. spathiger and N. battus.
Data on plant height (PH), panicle length (PL), flag leaf length (FL), flag leaf width, number of panicles (NPs) and seed morphology were recorded at the stage of maturity.
However, subsequent protein analysis showed that the SOX2 protein expression was completely eliminated, confirming successful knock-down.As shown in Figure 1C, distinct changes in cell morphology were recorded in 2102Ep and NTera-2 cells three days after siSOX2 transfection compared to cells transfected with a non-targeting siRNA control.
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