Characterization of compounds in vitro (including 9i; Mled1) led to the determination of key structural requirements for BIR2 binding affinity.
The effects of polysaccharides on plasma coagulation parameters in vitro including APTT, PT, TT and FIB were assayed and the results were described as follows.
There are several alternative methods for measuring mechanical properties of intact bone in vitro, including tension, torsion and three-point bending.
In recent years, a variety of organoids have been cultured successfully in vitro, including the stomach, liver, kidney, lung, gut, brain, and retina (Clevers, 2016).
There have been various attempts to produce multienzyme assemblies in vitro, including by gene fusion, protein or DNA scaffold construction, and chemical modification [3].
The expanded MSCs in the designed medium preserved differentiation potentials into three mesenchymal lineages in vitro, including chondrocytes, adipocytes and osteoblasts.
Results demonstrate that these molecules exert direct antimicrobial activity in vitro, including antibacterial activity of native IL-8 and MCP-1, and microbicidal activity of native IL-8.
Pol μ has been shown to participate in DNA synthesis at junctions in vitro, including on unpaired substrates, and to promote annealing.
Chemokines stimulate a variety of astrocyte responses in vitro, including cell migration, cytokine and chemokine production, and modulation of heterologous receptors.
Despite that, the peripheral CD4+ T cells expressing NefG2A show normal spontaneous proliferation in vivo or after stimulation in vitro, including in an allogenic mixed leukocyte reaction (MLR).
Many targets have been identified in vitro including FKHR, dynamin1, amphiphysin and tau protein [7], [8], [9].
