viral gene delivery are relatively simple compared to plasmid-based transfection techniques and data can be obtained more rapidly. Transfection efficiency is efficent and uniform, with each target cell carrying at least one copy of the CRE-NTR gene under the conditions employed. In addition, this work suggests that the sequential process of viral transduction, exposure of cells to reagents, and data acquisition can be transcribed into suitable automated and integrated workflow systems with standard liquid-handling dispensing units as well as image capture and data analysis workstations.
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3. Kozarsky, K.F. and Wilson, J.M., Gene therapy: adenovirus vectors. Curr. Opin. Genet.. Dev. 3, 499–503 (1993).
4. Lochmuller, H., et al., Emergence of early region 1-containing replication-competent adenovirus in stocks of replication-defective adenovirus recombinants (delta E1 + delta E3) during multiple passages in 293 cells. Hum. Gene Ther. 5, 1485–91 (1994).
5. Ng, P. et al., An enhanced system for construction of adenoviral vectors by the two plasmid rescue method. Hum. Gene Ther. 11, 693–699 (2000).
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PCR Performance Comparisons Between pfuturbo and Taq DNA
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pfuturbo DNA Polymerase:
A High-Performance, High-Fidelity Enzyme Ideal for PCR Cloning5.
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Unique Enhanced DNA Polymerase Delivers High Fidelity and Great PCR
Performance8.
Versatile Transfection Reagent Offers Low Toxicity and Consistent
Performance9.
Challenge the Performance of Your Hot-Start PCRs
with FastStart Taq DNA Polymerase and
the Novel FastStart High Fidelity PCR System10.
Highly Sensitive microRNA Array Performance11.
High Throughput RNA Isolation for High Performance Microarray Analysis