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. Author manuscript; available in PMC: 2014 Jul 1.
Published in final edited form as: FEBS J. 2013 Jun 7;280(14):10.1111/febs.12328. doi: 10.1111/febs.12328

Figure 9. N-terminal deletion mutant (6–45) is more active than hBD-3(wt) in blocking CXCR4.

Figure 9

Dose dependent inhibition of the SDF-1α-induced Ca2+-mobilization by hBD-3(wt) and mutant 6–45. Bar graph shows dose-dependent inhibition of high-affinity SDF-1α-binding by mutant 6–45.