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Parasite load was determined using a quantitative limiting-dilution assay as described previously [15].
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The hepatic and splenic parasite burdens were determined using a quantitative limiting dilution assay.
Single clone cells expressing CD26WT (MSTO-CD26WT), CD26/10Chi MSTO-CD26/10Chi MSTO-CD26/10Chiormock) were then selected using a standard limiting dilution method.
Clonal efficiency was assessed using a limiting dilution assay.
Single cell cloning was performed using a limiting dilution, and individual clones were established as cell lines.
To evaluate if lesion development was correlated with parasite multiplication at the site of infection, parasite load was quantified using a limiting dilution assay.
H413 cloned cell lines were established using a limit dilution method as described previously [ 28].
We isolated GFP-positive cells by using a limiting dilution method.
A cell line, HEI-OC1, was cloned in the absence of antibiotics, using a limiting dilution method, and characterized.
Single-cell cloning was carried out three times in positive hybridomas using a limiting dilution method until monoclones were obtained.
We tested tumour reconstitution in vivo using a limiting dilution of cells sorted from the SP and non-SP fractions.
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