Figure 1.
Figure 1. Screening of synthetic peptides derived from the second intracellular (i2) loops of S1P1 and S1P3. (A) Sequences of i2 loop–derived peptides and their activities in aortic ring assay. (B) Penetration into the cell. HUVECs were incubated with biotin-tagged KRX-725 for 10 and 30 minutes. Nonbiotinilated KRX-725 was used as control. Fixed and permeabilized cells were reacted with FITC-conjugated extravidin. Visualization was done using confocal microscope (axiovert M135; Zeiss). Micrographs were taken under × 63 objective.

Screening of synthetic peptides derived from the second intracellular (i2) loops of S1P1 and S1P3. (A) Sequences of i2 loop–derived peptides and their activities in aortic ring assay. (B) Penetration into the cell. HUVECs were incubated with biotin-tagged KRX-725 for 10 and 30 minutes. Nonbiotinilated KRX-725 was used as control. Fixed and permeabilized cells were reacted with FITC-conjugated extravidin. Visualization was done using confocal microscope (axiovert M135; Zeiss). Micrographs were taken under × 63 objective.

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