Table 1.

Mean fluorescence intensity values and percentage positive for mAb staining on BCD-treated cells

mAb specificitymAb cloneMFI (% positive)
ControlBCD
Nonspecific mIgG2b 2.92  (2.10) 3.18  (4.87)  
CD4 RPA-T4 403.9  (100) 410.9  (99.9)  
CD45 HI30 1425  (100) 1563  (100)  
CCR5, N-terminal CTC5 214.8  (100) 106.3  (99.1) 
CCR5, N-terminal 45502 10.03  (69.0) 7.55  (58.7) 
CCR5, MD 45523 56.8  (97.8) 43.6  (97.8)  
CCR5, MD 45549 8.54  (77.2) 5.16  (32.8)  
CCR5, ECL2 45531 393.6  (99.5) 56.1  (98.3) 
mAb specificitymAb cloneMFI (% positive)
ControlBCD
Nonspecific mIgG2b 2.92  (2.10) 3.18  (4.87)  
CD4 RPA-T4 403.9  (100) 410.9  (99.9)  
CD45 HI30 1425  (100) 1563  (100)  
CCR5, N-terminal CTC5 214.8  (100) 106.3  (99.1) 
CCR5, N-terminal 45502 10.03  (69.0) 7.55  (58.7) 
CCR5, MD 45523 56.8  (97.8) 43.6  (97.8)  
CCR5, MD 45549 8.54  (77.2) 5.16  (32.8)  
CCR5, ECL2 45531 393.6  (99.5) 56.1  (98.3) 

MFI, mean fluorescence intensity; mAb, monoclonal antibody; BCD, hydroxypropyl-β-cyclodextrin; MD, multidomain; ECL, extracellular loop.

Cells were treated with 20 mM BCD or untreated in phosphate-buffered saline for 1 hour at 37°C. The cells were then washed and stained for flow cytometry as described in “Materials and methods.” The data presented here are from histograms in Figure 4.

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