Fig. 4.
Fig. 4. Detection of KSHV gene sequences in BMDCs and PBDCs from MM patients and normal donors. DNA isolated from BMDCs from 15 MM patients and 6 normal donors was assayed for KSHV gene sequences by PCR using primers that amplify KS330233, followed by a nested PCR using primers internal to this sequence to yield a final PCR product of 186 bp. Results from 10 MM patient BMDCs (lanes 2 through 11) and 3 normal donor BMDCs (lanes 12 through 14) are shown in (A). (B) Results of PCR on PBDCs DNA from 5 MM patients (lanes 2 through 6) and 4 normal donors (lanes 7 through 10). In each case DNA from BCBL-1 cell line (lane 1) served as the positive control. β-Actin was amplified in all samples to ensure adequacy and integrity of DNA.

Detection of KSHV gene sequences in BMDCs and PBDCs from MM patients and normal donors. DNA isolated from BMDCs from 15 MM patients and 6 normal donors was assayed for KSHV gene sequences by PCR using primers that amplify KS330233, followed by a nested PCR using primers internal to this sequence to yield a final PCR product of 186 bp. Results from 10 MM patient BMDCs (lanes 2 through 11) and 3 normal donor BMDCs (lanes 12 through 14) are shown in (A). (B) Results of PCR on PBDCs DNA from 5 MM patients (lanes 2 through 6) and 4 normal donors (lanes 7 through 10). In each case DNA from BCBL-1 cell line (lane 1) served as the positive control. β-Actin was amplified in all samples to ensure adequacy and integrity of DNA.

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