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Flow cytometric analysis of CD68 expression by activated F4/80-positive mouse peritoneal macrophages. C57BL/6 mouse thioglycolate-elicited peritoneal exudate cells (PECs) were harvested and fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution (Cat. No. 554722). The cells were then washed and stained in BD Perm/Wash™ Buffer (Cat. No. 554723) with BD Horizon™ BV421 Rat Anti-Mouse F4/80 antibody (Cat. No. 565411) and either PE Rat IgG2a, κ Isotype Control (Cat. No. 553930; dashed line histogram) or PE Rat Anti-Mouse CD68 antibody (Cat. No. 566386/ 566387; solid line histogram) at 0.25 μg/test. The fluorescence histogram showing CD68 expression (or Ig Isotype control staining) was derived from F4/80 positive-gated events with the forward and side light-scatter characteristics of intact PECs. Flow cytometric analysis was performed using a BD LSRFortessa™ X-20 Cell Analyzer System. Data shown on this Technical Data Sheet are not lot specific.
Flow cytometric analysis of CD68 expression by activated F4/80-positive mouse peritoneal macrophages. C57BL/6 mouse thioglycolate-elicited peritoneal exudate cells (PECs) were harvested and fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution (Cat. No. 554722). The cells were then washed and stained in BD Perm/Wash™ Buffer (Cat. No. 554723) with BD Horizon™ BV421 Rat Anti-Mouse F4/80 antibody (Cat. No. 565411) and either PE Rat IgG2a, κ Isotype Control (Cat. No. 553930; dashed line histogram) or PE Rat Anti-Mouse CD68 antibody (Cat. No. 566386/ 566387; solid line histogram) at 0.25 μg/test. The fluorescence histogram showing CD68 expression (or Ig Isotype control staining) was derived from F4/80 positive-gated events with the forward and side light-scatter characteristics of intact PECs. Flow cytometric analysis was performed using a BD LSRFortessa™ X-20 Cell Analyzer System. Data shown on this Technical Data Sheet are not lot specific.
Flow cytometric analysis of CD68 expression by activated F4/80-positive mouse peritoneal macrophages. C57BL/6 mouse thioglycolate-elicited peritoneal exudate cells (PECs) were harvested and fixed and permeabilized using BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution (Cat. No. 554722). The cells were then washed and stained in BD Perm/Wash™ Buffer (Cat. No. 554723) with BD Horizon™ BV421 Rat Anti-Mouse F4/80 antibody (Cat. No. 565411) and either PE Rat IgG2a, κ Isotype Control (Cat. No. 553930; dashed line histogram) or PE Rat Anti-Mouse CD68 antibody (Cat. No. 566386/ 566387; solid line histogram) at 0.25 μg/test. The fluorescence histogram showing CD68 expression (or Ig Isotype control staining) was derived from F4/80 positive-gated events with the forward and side light-scatter characteristics of intact PECs. Flow cytometric analysis was performed using a BD LSRFortessa™ X-20 Cell Analyzer System. Data shown on this Technical Data Sheet are not lot specific.
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
The FA/11 monoclonal antibody specifically binds to CD68 which is also known as Macrosialin, Lamp4 or Scard1. CD68 is a heavily glycosylated ~ 85-115 kDa type I transmembrane protein that belongs to the lysosomal-associated membrane protein (LAMP) family. Although it is expressed at the cell surface, it is predominantly expressed as an intracellular protein in late endosomes. CD68 is expressed by macrophages, Kupffer cells, histiocytes, microglia, and is considered a useful pan-macrophage marker. It is also expressed by dendritic cells, Langerhans cells and osteoclasts. CD68 expression is upregulated and its glycosylation patterns can be changed by proinflammatory agents. Although CD68 binds to oxidized low-density lipoproteins, its exact biological function is not well defined.
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Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Refer to manufacturer's instructions for use and related User Manuals and Technical Data Sheets before using this product as described.
Comparisons, where applicable, are made against older BD technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.