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. Author manuscript; available in PMC: 2009 Apr 13.
Published in final edited form as: AIDS Res Hum Retroviruses. 2005 Apr;21(4):273–284. doi: 10.1089/aid.2005.21.273

FIG. 1.

FIG. 1

(A) Schematic illustration of lentiviral vector expressing both p12I-HA and GFP (sample vector) as bicistronic messages and GFP alone (control vector) from elongation factor 1α promoter. Abbreviations: LTR, long terminal repeats; RRE, Rev response element; EFIα, elongation factor 1α promoter; IRES, internal ribosome entry site; WPRE, woodchuck hepatitis posttranscriptional regulatory element. (B) Flow cytometric analysis illustrating the expression of GFP in Jurkat T cells 7 days postinfection with lentiviral vectors. Both sample (expressing p12I-HA and GFP) and control (GFP alone) groups contain relatively high and similar levels of GFP. (C) RT-PCR demonstrating the expression of p12I-HA in Jurkat T cells 7 days postinfection with lentiviral vectors. Jurkat cells spin infected with sample vector express p12I whereas control vector spin-infected cells do not express p12I. RT-PCR was performed with triplicate samples and controls. GAPDH was used as a control for the integrity of the message.