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Blood, Vol. 106, Issue 3, 893-898, August 1, 2005
Efficient marking of human cells with rapid but transient repopulating activity in autografted recipients
Blood Glimm et al.
106: 893
Supplemental materials for: Glimm et al, Vol 106, Issue 3, 893-898
Files in this Data Supplement:
- Table S1. LAM-PCR analysis of all provirus insertion sites (PDF, 270 KB) -
All patient samples analyzed were derived from cloned and sequenced PB LAM products as shown in Figure 1. Each sequenced LAM-PCR amplicon was aligned to the Human Genome Database and the insertion site identified using University of California–Santa Cruz BLAT search tools. Integrant-host-junction sequences were present in the first 15 nucleotides of the genomic DNA flanking the 5'LTR (10 nucleotides). Genomic length denotes the size of the LAM-PCR amplicon without linker and LTR sequences. Pat indicates patient number; WBC, white blood cells; and (G), purified granulocytes.
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