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In contrast to blood leukocytes, non-stimulated BALF leukocytes showed a very high basal activation when stimulated in vitro.
The biomimetic tissues could maintain functional contraction and be electrically stimulated in vitro for 28 days.
Primary activated human HSC were stimulated in vitro for 24 h with SE in the indicated doses.
Lymphocytes were stimulated in vitro with PHA (a), tetanus antigen (b), and adenovirus antigen (c) as described.
dA2GIP-Oxm was resistant to DPP-IV and significantly stimulated in vitro insulin release.
Here we report that central nervous system neurons patterned on large enough one-dimensional rings can be magnetically stimulated in vitro.
Spleen cells from BALB/c mice (H-2d) immunized with gD2, formulated with or without AlPO4 and/or IL-12, were stimulated in vitro with overlapping gD2 peptides.
On the other hand, PEPB significantly stimulated in vitro proliferation of mouse splenocytes in a dose-dependent manner within the testing range from 32.5 to 500 μg/ml.
Peripheral blood mononuclear cells (PBMC) were isolated and stimulated in vitro with IFNß.
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No proliferation was seen when splenocytes isolated from PBS immunized mice were stimulated in-vitro with any of the recombinant proteins using any concentration.
Therefore, sorted B cells were stimulated in-vitro with various concentrations of HEL together with a sub-mitogenic concentration of LPS.
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