Exact(11)
b Comparison of the signal strengths from MR images using T2WI before and after the injection of the control or HPA&GoldMag probes in nude mice.
No fluorescence was detectable after injection of the control peptide.
Injection of the control MO did not affect the morphology (Figure 3A, b).
It has been previously shown [4] that the injection of the control peptide does not yield functional CD4 Tregs.
Following injection of the control LNT.shGFP virus in vivo, basal levels of ZONAB in RPE cells and ZO-1 immunofluorescence at cell-cell junctions were observed (Fig. 2A,B).
Intrathecal injection of the control antibody (IgG) into infant SNI mice did not induce significant changes in mechanical thresholds.
Similar(49)
Optical imaging data showed that binding of the HVGGSSV peptide within the irradiated tumors was not affected by pre-injection of the control IgGs.
Group 1 mice were given injections of 1 × 105 CT26.WT mouse colon carcinoma cells transfected with nonspecific control siRNA duplexes, and were subsequently given injections of the control siRNA twice weekly.
Injection of the scrambled control siRNA did not disrupt nerve cord development (Fig. 4A, Table 1).
Moreover, this head-specific homing of Cy5.5Angiopep-2 wasignificantlyly greater than that observed after injection of the negative control Cy5.5Angiopep-7.
Upon intrascrotal injection of the positive controls, LPS or TNFα, there were approximately 12 15 leukocytes adherent (Fig. 6A) within the post-capillary venules and 30 leukocytes that had emigrated (Fig. 6B) into the tissue, 4 hours post-stimulation.
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