Fig. 5.
Fig. 5. Exogenous gene expression in mice treated with primary B cells infected with MPL-PURO vector virus-expressing PLP. / (A) RT-PCR was performed on total RNA extracted from the spleens of mice treated with MPL-PURO–infected B cells (lanes 2-7) and mice treated with B cells infected with the control vector MML-PURO (lanes 8 and 9). An untreated mouse was used as negative control (lane 10), and a MPL-PURO–infected WEHI 231 B-cell line was used as positive control (lane 1). PA indicates paralysis. (B) RT-PCR with the use of MML-specific primers was performed on total RNA extracted from the spleens of mice treated with MML-PURO–infected B cells, lanes 1 and 2. RNA extracted from the spleen of an untreated mouse (lane 3) and from MPL-PURO–infected WEHI 231 B cells (lane 4) were used as negative controls. For all samples, amplification of the housekeeping geneGAPDH was performed to ensure that equal levels of total RNA were used.

Exogenous gene expression in mice treated with primary B cells infected with MPL-PURO vector virus-expressing PLP.

(A) RT-PCR was performed on total RNA extracted from the spleens of mice treated with MPL-PURO–infected B cells (lanes 2-7) and mice treated with B cells infected with the control vector MML-PURO (lanes 8 and 9). An untreated mouse was used as negative control (lane 10), and a MPL-PURO–infected WEHI 231 B-cell line was used as positive control (lane 1). PA indicates paralysis. (B) RT-PCR with the use of MML-specific primers was performed on total RNA extracted from the spleens of mice treated with MML-PURO–infected B cells, lanes 1 and 2. RNA extracted from the spleen of an untreated mouse (lane 3) and from MPL-PURO–infected WEHI 231 B cells (lane 4) were used as negative controls. For all samples, amplification of the housekeeping geneGAPDH was performed to ensure that equal levels of total RNA were used.

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