LiFluor™ 568-X-dUTP can be enzymatically incorporated into DNA with Reverse Transcriptases, Taq DNA Polymerase, phi29 DNA Polymerase, Klenow Fragment, exo-, Klenow Fragment, and DNA Polymerase I. The X linker between LiFluor™ 568 and dUTP can improve..

LiFluor™ 568-X-UTP can be enzymatically incorporated into RNA with T7, T3 and SP6 RNA polymerases, as well as other RNA modifying enzymes. The X linker between LiFluor™ 568 and UTP can improve the incorporation efficiency.   Key Features • Bri..

LiFluor™ 594-X-dUTP can be enzymatically incorporated into DNA with Reverse Transcriptases, Taq DNA Polymerase, phi29 DNA Polymerase, Klenow Fragment, exo-, Klenow Fragment, and DNA Polymerase I. The X linker between LiFluor™ 594 and dUTP can improve..

LiFluor™ 594-X-UTP can be enzymatically incorporated into RNA with T7, T3 and SP6 RNA polymerases, as well as other RNA modifying enzymes. The X linker between LiFluor™ 594 and UTP can improve the incorporation efficiency.   Key Features • Bri..

LiFluor™ 647-X-dUTP can be enzymatically incorporated into DNA with Reverse Transcriptases, Taq DNA Polymerase, phi29 DNA Polymerase, Klenow Fragment, exo-, Klenow Fragment, and DNA Polymerase I. The X linker between LiFluor™ 647 and dUTP can improve..

LiFluor™ 647-X-UTP can be enzymatically incorporated into RNA with T7, T3 and SP6 RNA polymerases, as well as other RNA modifying enzymes. The X linker between LiFluor™ 647 and UTP can improve the incorporation efficiency.   Key Features • Bri..

Lentivirus Transduction Enhancer I is a novel chemical reagent that increases lentiviral transduction efficiency into in vitro systems. Normally, incubation of lentivirus particles in cells in the presence ofpolybrene is generally efficient in t..

Lentivirus Transduction Enhancer II is a nontoxic novel chemical reagent that increases lentiviraltransduction efficiency by modulating membrane permeability. Normally, incubation of lentivirusparticles in cells in the presence of polybrene is genera..