LEDGF Monoclonal Antibody, 50ul Aspirating Pipets which always presents with retinal
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LEDGF Monoclonal Antibody, 50ul Aspirating Pipets which always presents with retinalA chromosomal aberration involving PSIP1 is associated with pediatric acute myeloid leukemia (AML) with intermediate characteristics between M2 M3 French American British (FAB) subtypes. Translocation t(9 11)(p22 p15) with NUP98. The chimeric transcript is an in frame fusion of NUP98 exon 8 to PSIP1 LEDGF exon 4.,domain: Residues 340 417 are necessary and sufficient for the interaction with HIV 1 IN (IBD domain).,function: Transcriptional coactivator
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