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Dexamethasone (#D1756, Sigma) was used to induce cell death in thymocytes (1 μM).
The anti-Fas mAb CH11 was used to induce cell apoptosis and the cell apoptosis was assayed using Hoechst 33342 staining as described previously [36], [59].
In this study we investigated the TG2 – cell death relationship focusing on three of these variables: i) its conformation/activity state, ii) localization (nuclear or cytoplasmic) and iii) the type of stressor used to induce cell death.
Polyethylene glycol (PEG) was used to induce cell fusion.
In these studies, glutamate, lipopolysaccharide, and hydrogen peroxide (H2O2), respectively, were used to induce cell injuries.
The SYTOX Green staining experiment indicated that the system can be used to induce cell death by green-light exposure.
Similar(49)
HSVtk and GCV have been used to induce apoptotic cell death in cell culture or tissues.
As a classical polyclonal stimulator acting through T-cell receptor complex (TCR -CD3 complex, PHA has been used TCR -CD3e T complextivation and stimulate IL-2 secretion, which is dePHAdent on an increase of [Ca2+]i[ 41, 42].
Quiescent T cell are relatively refractory to genetic modification and a variety of activation reagents have been used to induce T cell division, including phytohaemagglutinin, OKT3 and magnetic beads conjugated with anti-CD3 and anti-CD28 antibodies.
In conclusion, our study is a proof of concept that chemical cocktails could be used to induce somatic cell reprogramming in vivo and our chemical combination provides a starting point for further optimization to induce cardiac regeneration.
The activating anti-Fas antibody was used to induce Jurkat cell apoptosis at 10 µg/ml.
More suggestions(15)
used to trigger cell
exist to induce cell
suggested to induce cell
used to manipulate cell
used to induce brain
used to analyze cell
used to induce fatigue
used to label cell
used to assess cell
used to prevent cell
used to infer cell
used to block cell
used to induce seedlessness
used to induce sedation
used to extrapolate cell
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