Table 1.
Line | MFI
|
% lysis of 1106 mel | |
---|---|---|---|
Control | CD16 | ||
3G8 dim | |||
E4 | 10 | 17 | 6 |
C1 | 11 | 25 | 5 |
C10 | 10 | 33 | 3 |
C11 | 10 | 36 | 2 |
G11 | 12 | 19 | 3 |
D12 | 9 | 41 | 3 |
D3 | 10 | 33 | 2 |
H1 | 11 | 28 | 12 |
Mean | 10.3 | 29 | 4.5 |
3G8 bright | |||
17 | 10 | 184 | 34 |
24 | 11 | 207 | 28 |
3–2 | 12 | 199 | 29 |
4–2 | 11 | 296 | 37 |
30 | 12 | 261 | 32 |
32 | 10 | 171 | 31 |
33 | 9 | 184 | 42 |
334 | 9 | 314 | 28 |
Mean | 10.5 | 227 | 32.6 |
NK cells lines were sorted (30 cells per well) to be either 3G8 dim (upper half of the table) or 3G8 bright (lower half of the table). Median fluorescence intensity (MFI) was determined by using FACS analysis. Assays were performed at an E:T ratio of 2.5:1. The table shows one representative experiment out of three performed.