Figure 2
Figure 2. Identification of soluble ULBP1 (sULBP1) in AML plasma. (A) ULBP1 ELISA was established (see “Analysis of soluble ULBP1”) and used to detect sULBP1 in C1R-ULBP1 cells (lane 1, culture supernatant gray bar; lane 2, cell lysate, black bar) but not in control C1R-neo cells (lanes 3 and 4). (B) Immunoprecipitation and Western analysis of sULBP1 in cell lysates of C1R-neo control cells (lane 1) C1R-ULBP1 cells (lane 2) and rh ULBP1/Fc (55 kDa; 3 ng, lane 3). Black arrow indicates the full-length ULBP1 molecule of approximately 40 kDa. (C,D) Levels of sULBP and sMICA in plasma from AML patients (n = 43; open symbols) and healthy donors (HD; n = 25; closed symbols), as determined by ELISA. Horizontal bars show the median values. Not significant (P = not significant) or highly significant (P < .001) difference in sULBP1 and sMICA levels in AML versus HD, respectively.

Identification of soluble ULBP1 (sULBP1) in AML plasma. (A) ULBP1 ELISA was established (see “Analysis of soluble ULBP1”) and used to detect sULBP1 in C1R-ULBP1 cells (lane 1, culture supernatant gray bar; lane 2, cell lysate, black bar) but not in control C1R-neo cells (lanes 3 and 4). (B) Immunoprecipitation and Western analysis of sULBP1 in cell lysates of C1R-neo control cells (lane 1) C1R-ULBP1 cells (lane 2) and rh ULBP1/Fc (55 kDa; 3 ng, lane 3). Black arrow indicates the full-length ULBP1 molecule of approximately 40 kDa. (C,D) Levels of sULBP and sMICA in plasma from AML patients (n = 43; open symbols) and healthy donors (HD; n = 25; closed symbols), as determined by ELISA. Horizontal bars show the median values. Not significant (P = not significant) or highly significant (P < .001) difference in sULBP1 and sMICA levels in AML versus HD, respectively.

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