Fig. 2.
![Fig. 2. Flow cytometric analysis of CXCR-1 and CXCR-2 expression on neutrophils. Cells were incubated with α-CXCR–1 antibody SE-2 (A) or with α-CXCR–2 antibody RII115 (B). Incubation with either antibody was performed in the absence (1) or presence (2) of a 100-fold molar excess of the peptide fragments CXCR-1[1-30] (A) or CXCR-2[6-29] (B). Subsequently, cell-bound antibodies were detected by fluorescein-conjugated goat α-mouse IgG. Control cells received the secondary antibody only (3).](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/90/11/10.1182_blood.v90.11.4588/3/bl_0034f2.jpeg?Expires=1735814099&Signature=hDupEbfqAH~cHk5GE1ne6RfGQGOIZKhgYb~FtHV2aZrlsUxK6tXXtaQ1qL76JNbycd2nuAp5eIzqB2KNyk5z7ZdH-ucnFCSYjAYbTg240bVsVnJJ2SAGzAq4loIHEVYmjaYfRxUlim3~fu4pkx7d5IRG3UK2wygdNxQeotIQNabGDdAPOcwpKEVsm~1HUnbP7V-r0OHj~KZbVl7fxBCJ6QH~phcUdRErI8hNAa8G0y8vzqgKy9Q8VP-cNj3QMGiz7vextmzq4zX62ssUyVVVAtxa6-SJnf6ZyTuTFBNOb-~SrqusSIJuJEdEhTMvvlzpPgQOYTywKb9Zs9zehjncgg__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)
Flow cytometric analysis of CXCR-1 and CXCR-2 expression on neutrophils. Cells were incubated with α-CXCR–1 antibody SE-2 (A) or with α-CXCR–2 antibody RII115 (B). Incubation with either antibody was performed in the absence (1) or presence (2) of a 100-fold molar excess of the peptide fragments CXCR-1[1-30] (A) or CXCR-2[6-29] (B). Subsequently, cell-bound antibodies were detected by fluorescein-conjugated goat α-mouse IgG. Control cells received the secondary antibody only (3).
