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However the physician will use the same assay also for exclusion of DVT [ 14].
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Here we use the same assays to ask which MBONs are required for visual memory.
Here we use the same assays in combination with investigation of the intracellular concentration to obtain a more detailed picture of the function of the TI domain.
However, for results to be truly comparable to those reported by us, antibody titres among such patients would need to be assessed using the same assay, preferably performed at the same time and under the same laboratory conditions.
We have used the same assay as in [41], to minimize interassay variation.
Additionally the (S -3-HB negative control S -3-HBno reS -3-HBusinegativeame assay kit.
This agrees with previous data showing that Polβ overproduction increases (up to 4-fold) mutagenesis using the same assay [33].
Previous studies support our findings, reporting variability between different assays as well as inter-laboratory differences using the same assay [16], [17], [18], [19], [21].
Using the same assay, variable strengths of binding were observed for the SmTK3 constructs, depending on the extent of the N-terminal deletion (Fig. 7).
We used the same assay to determine the sequences within the HCF-1N Basic region required to support tsBN67 cell proliferation at 40°C.
This result was similar to the enzyme activity measured in rXylanase expressed in E. coli (10.2 nmol/min/µg protein) and commercial Trichoderma viride xylanase (2.3 nmol/min/µg of protein) using the same assay conditions.
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