CD87 Antibody / uPAR (RQ4654)

CD87 Antibody Human PBMC FACS. Flow cytometric analysis of human peripheral blood mononuclear cells (PBMCs) using CD87 Antibody. Cells were detected with a fluorescently conjugated secondary antibody and compared against isotype control. CD87 Antibody, recognizing uPAR/PLAUR, demonstrates a clear positive shift consistent with CD87 expression on immune cell populations, including activated monocytes and other leukocyte subsets involved in inflammatory responses and immune regulation.

CD87 Antibody Human Immune Cell FACS. Flow cytometric analysis of human peripheral blood mononuclear cells (PBMCs) using CD87 Antibody. Cells were blocked and detected with a fluorescently conjugated secondary antibody. CD87 Antibody, recognizing uPAR/PLAUR, demonstrates a clear positive shift compared to isotype control, confirming CD87 expression on immune cell populations and supporting its use for studying immune activation, leukocyte migration, and uPAR-mediated inflammatory signaling.

CD87 Antibody Human Cancer Cell FACS. Flow cytometric analysis of human SiHa cells using CD87 Antibody at 1 ug/million cells. Cells were blocked with goat serum and compared against cells alone (red) and isotype control (green). CD87 Antibody, recognizing uPAR/PLAUR, demonstrates a clear positive shift (blue) confirming CD87 expression in SiHa cells and supporting its use for studying uPAR-mediated cell signaling, migration, and cancer cell invasion pathways.

CD87 Antibody Human Cell and Tissue WB. Western blot analysis of human samples using CD87 Antibody at 0.5 ug/ml. Lane 1: human placenta tissue lysate, Lane 2: human U-2 OS cell lysate, Lane 3: human A431 cell lysate, Lane 4: human HeLa cell lysate, Lane 5: human A549 cell lysate. An HRP-conjugated secondary antibody with ECL substrate was used for detection. CD87 Antibody, recognizing uPAR/PLAUR, detects a prominent band at approximately 39 kDa, consistent with the expected molecular weight of the uPA receptor. This result supports detection of CD87, a cell surface receptor involved in immune cell activation, extracellular matrix remodeling, and cell migration signaling.

CD87 Antibody Mouse and Rat WB. Western blot analysis of mouse and rat samples using CD87 Antibody at 0.5 ug/ml. Lane 1: rat testis tissue lysate, Lane 2: mouse small intestine tissue lysate, Lane 3: mouse kidney tissue lysate, Lane 4: mouse testis tissue lysate. An HRP-conjugated secondary antibody with ECL substrate was used for detection. CD87 Antibody, recognizing uPAR/PLAUR, detects a prominent band at approximately 39 kDa, consistent with the expected molecular weight of the uPA receptor. This result supports detection of CD87, a cell surface receptor involved in immune regulation, extracellular matrix remodeling, and cell migration pathways.