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Gross, G. W. Simultaneous single unit recording in vitro with a photoetched laser deinsulated gold multimicroelectrode surface.
The active diastereomer of MMV-08138 directly inhibited PfIspD activity in vitro with a 50% inhibitory concentration (IC50) of 7.0 nM.
Experimental validations showed that OmpGF could refold in vitro with a predominant β-sheet structure, as confirmed by circular dichroism.
In fact, the human p58C does bind nucleic acids in vitro, with a preference for ssRNA/dsDNA junction substrates (Vaithiyalingam et al., 2010).
I-125-labeled cRGD-GNPs was stable in vitro, with a stability of 86.2% ± 1.7% in PBS and 76.3% ± 1.6% in 10% FBS at 3 days after labeling.
Furthermore, citrate-coated GNPs that had a low radiosensitization effect in vitro with a DEF of 1.08 promoted a delay in tumour growth in B16F10 murine melanoma model.
Isolates 124A and 140A were tested in vitro with a macrophage cell line.
However, what occur in vitro with a cell line may only approximate the whole tissue's response to radiation damage.
KAP1 contains an N-terminal protein interaction domain (the RBBC domain) that can interact in vitro with a KRAB domain [30], [31].
In comparison with producing dsRNA in vitro with a kit, bacterially expressed dsRNA is more cheaply and is more easily used in large scale gene function analysis [15].
The Smac dimer is highly stable in vitro with a dissociation constant (Kd) of 34×10−21 M [11], which may preclude monomer exchange with dimeric Smac.
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