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Area A was analyzed further to investigate dose dependence.
To examine whether KT-NB treatment can alter important components involved in the mitotic spindle poles, the localization of Aurora A was analyzed.
Recombinant TbUGP (0.75 mg/mL in buffer A) was analyzed by sedimentation velocity using a Beckman Optima XL-1 Analytical Ultracentrifuge with an AN50-Ti rotor at 32,000 rpm at 20°C.
After measuring the baseline with HBS-EP buffer (pH 7.4), association with Protein A was analyzed by injection of Fc samples (HBS-EP buffer), followed by analysis of the dissociation of the Fc proteins from Protein A by injection of HBS-EP buffer only.
A standard viral dynamic model, shown schematically in Figure 2 A, was analyzed in which infected cells in the eclipse phase, I1, transition to productive infection, I2, and with both populations as well as long-lived infected cells, M*, being potential targets of immune cell killing.
The adjacency matrix, A, was analyzed by WGCNA with minModuleSize = 60 to obtain the gene modules (Langfelder and Horvath 2008).
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The level of LDH-A was analyzed by densitometry scanning of appeared band on gel using Alpha image analyzer software.
The risk of IGR and type 2 diabetes in relation to quartiles of serum fetuin-A was analyzed by using multinomial logit models.
Activity of LDH-A was analyzed by activity gel assay.
Cell migration toward VEGF-A was analyzed using a Boyden chamber (Neuro Probe, Gaithersburg, MD, USA), as previously described.
The 2,3-BD produced by strain 10-1-A wanalyzedzed by GC with a flame ionization detector and a fused silica capillary column [ 24].
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