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  Indian J Med Microbiol
 

Figure 1: Representative images showing proliferation of lymphocytes stained with carboxyfluorescein succinimidyl ester (CFSE) following in vitro stimulation with autoantigens, insulin (10.0 μg/ml) and glutamic acid decarboxylase 65 (GAD65, 5.0 μg/ml), positive control, phytohaemagglutinin (PHA, 5.0 μg/ml) and negative control, media control (MC). (A) Lymphocytes were gated according to forward and side scatter. Histograms represent cells stimulated with (B) PHA, (C) media control, (D) insulin, (E) GAD65.

Figure 1: Representative images showing proliferation of lymphocytes stained with carboxyfluorescein succinimidyl ester (CFSE) following <i>in vitro</i> stimulation with autoantigens, insulin (10.0 μg/ml) and glutamic acid decarboxylase 65 (GAD65, 5.0 μg/ml), positive control, phytohaemagglutinin (PHA, 5.0 μg/ml) and negative control, media control (MC). (<b>A</b>) Lymphocytes were gated according to forward and side scatter. Histograms represent cells stimulated with (<b>B</b>) PHA, (<b>C</b>) media control, (<b>D</b>) insulin, (<b>E</b>) GAD65.