Figure 4
Figure 4. Reduced expression of AP3δ affects the stability of the AP3 complex. Western blot analysis of lysates from magnetically activated cell sorter (MACS) –purified CD8 T cells of 2 healthy controls: an AP3β3A-deficient patient and the index patient (lanes 1-4). Two separate blots are shown that used rabbit antibodies against AP3δ and AP3σ (left) and AP3β and AP3μ (right). β-actin was used as a loading control. AP3δ protein was analyzed by using 2 different antibodies23,24 in 3 independent experiments with similar results. Lanes 5 and 6 show blots from patient PHA/IL-2 blasts retrovirally transduced with an AP3D1-expressing or empty vector analyzed in the same experiment. These cells were sorted by using fluorescence-activated cell sorting (FACS) for GFP-positive cells to enrich for successfully transduced cells.

Reduced expression of AP3δ affects the stability of the AP3 complex. Western blot analysis of lysates from magnetically activated cell sorter (MACS) –purified CD8 T cells of 2 healthy controls: an AP3β3A-deficient patient and the index patient (lanes 1-4). Two separate blots are shown that used rabbit antibodies against AP3δ and AP3σ (left) and AP3β and AP3μ (right). β-actin was used as a loading control. AP3δ protein was analyzed by using 2 different antibodies23,24  in 3 independent experiments with similar results. Lanes 5 and 6 show blots from patient PHA/IL-2 blasts retrovirally transduced with an AP3D1-expressing or empty vector analyzed in the same experiment. These cells were sorted by using fluorescence-activated cell sorting (FACS) for GFP-positive cells to enrich for successfully transduced cells.

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