Fig. 1.
Fig. 1. (A) Structure of the retroviral vectors used to transduce murine bone marrow. The LTRs and vector backbone for all constructs was MSCV2.2. The EcoRI and Xba I restriction enzyme sites used for determining proviral integration are indicated. (B) Protocol for retroviral transduction of FU-treated bone marrow and subsequent reconstitution. During the 48-hour cocultivation, retroviral supernatants were added to the media (1 mL every 24 hours) or cells were transduced by spin infection without cocultivation (see Materials and Methods).

(A) Structure of the retroviral vectors used to transduce murine bone marrow. The LTRs and vector backbone for all constructs was MSCV2.2. The EcoRI and Xba I restriction enzyme sites used for determining proviral integration are indicated. (B) Protocol for retroviral transduction of FU-treated bone marrow and subsequent reconstitution. During the 48-hour cocultivation, retroviral supernatants were added to the media (1 mL every 24 hours) or cells were transduced by spin infection without cocultivation (see Materials and Methods).

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