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. 2002 Jun;106(2):159–172. doi: 10.1046/j.1365-2567.2002.01422.x

Table 1. Specificity of monoclonal antibodies (mAbs) against guinea-pig CD1 proteins.

Guinea-pig CD1 isoforms

mAbs Derived against b1 b2 b3 b4 c1 c2 c3
CD1F2/5E3 Guinea-pig CD1 ± ++ + ++ ++ +
CD1F2/6B5 Guinea-pig CD1 + ++ ++ + ++ ++ +
CD1F2/1B12 Guinea-pig CD1 ++ ++ ++ +
CD1·4-1D12 Guinea-pig CD1 +
Msgp9 Guinea-pig CD1 ++
7C4 Human CD1b + +
WM25 Human CD1b ++
BCD1b1 Human CD1b ++ +
BCD1b2 Human CD1b ++ ++ ++ +
BCD1b3 Human CD1b ++ ++ ++ ± +
BCD1b4 Human CD1b ++ ++
CD1d69 Human CD1d ±∼ +*
20–27 Sheep CD1 ++ ++ ±
CC-20 Cow CD1 ++ + ++
Fe5·5C1 Feline CD1 ++ ± ++ ++ +

New mAbs generated in this study and mAbs against CD1 of human or other species were tested for their reactivity with guinea-pig CD1 (gpCD1) proteins using transfectants of guinea-pig cell lines 104C1 and GPC-16 expressing individual isoforms of gpCD1. All mAbs were mouse immunoglobulin G (IgG) and were detected with anti-mouse IgG/IgM-conjugated to fluorescein isothiocyanate (FITC) as a secondary reagent. Symbols signify the following: ‘−’, no reactivity above the level of isotype-matched non-binding control antibody; ‘±’, weak but significant shift from isotype-matched control antibody; ‘+’, positive staining with a mean fluorescence intensity (MFI) of 10–100; ‘++’, strong staining with a MFI of >100.

*

gpCD1b4 expression detected by CD1d69 was ‘+’ in GPC-16 cells transfected with gpCD1b4 and ‘±’ in 104C1 transfectant cells.