Table 4.

Gene Marking Frequency

Transduction4-150
LIFLIF [+AZT]4-151SCF
CoH-1 CFU-C 4 (4/90) 1 (1/78) 8 (7/90) 
 LTC-CFC 2 (2/90) 2 (2/92) 2 (2/90) 
CoH-2 CFU-C 3 (3/91) 2 (2/91) 2 (2/91) 
 LTC-CFC 4 (4/92) 3 (3/90) 3 (3/86) 
CoH-3 CFU-C 4 (3/84) 2 (2/91) 6 (5/90) 
 LTC-CFC 6 (5/88) 2 (2/92) 1 (1/91) 
Transduction4-150
LIFLIF [+AZT]4-151SCF
CoH-1 CFU-C 4 (4/90) 1 (1/78) 8 (7/90) 
 LTC-CFC 2 (2/90) 2 (2/92) 2 (2/90) 
CoH-2 CFU-C 3 (3/91) 2 (2/91) 2 (2/91) 
 LTC-CFC 4 (4/92) 3 (3/90) 3 (3/86) 
CoH-3 CFU-C 4 (3/84) 2 (2/91) 6 (5/90) 
 LTC-CFC 6 (5/88) 2 (2/92) 1 (1/91) 

Retroviral gene marking, determined by neo (neomycin phosphotransferase) gene DNA PCR, is expressed as a percentage and the number of neo-positive colonies divided by the total number of β-globin–positive colonies is indicated in parentheses.

F4-150

Supernatant transduction was performed in the presence of IL-3, IL-6, and LIF (LIF) or IL-3, IL-6, and SCF (SCF). For details, see the Materials and Methods.

F4-151

Cells were plated after transduction in methylcellulose (CFU-C) or cultured on Sys1 mouse stromal cells (LTC-CFC) in the presence of AZT.

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