Sentence examples for vitro with each from inspiring English sources

Retinae were then electroporated in vitro with each reporter and RFP/GAPDH-shRNA, using the ventral fissure and optic nerve head as landmarks.

In order to determine the underlying gene networks and processes involved in primordial follicle development, microarray analysis was performed on RNA from whole rat ovaries treated for two days in vitro with each of the above listed growth factors independently.

The PBMCs were stimulated in vitro with each of the Lck-derived peptides or with a control peptide.

The PBMC of the HLA‐A2+ cancer patients were then stimulated in vitro with each of these 17 peptides followed by examination of their IFN‐γ secretion.

Taken together, these results indicate that the PBMCs that were stimulated in vitro with each of the Lck90−99, Lck449−458, and Lck450−458 peptides can exhibit cytotoxicity against cancer cells in an HLA-A11-, -A31-, or -A33-restricted manner.

The PBMCs from HLA-A11+ patients (patients 2, 6, and 3), which were stimulated in vitro with each of the Lck90−99, Lck449−458, and Lck450−458 peptides, exhibited higher levels of cytotoxicity against HLA-A11+ SQ-1 cells than against HLA-A11− COLO 201 cells and HLA-A11+ PHA-stimulated T-cell blasts.

We further investigated which asexual clusters are differentially expressed between infection and in vitro culture by comparing the in vitro transcriptomes with each of the three field datasets separately.

We then determined whether or not the CTLs induced by in vitro stimulation with each of the Lck90−99, Lck449−458, and Lck450−458 peptides could show cytotoxicity against cancer cells.

A total of 36 peptides with high binding scores to HLA-A2 (A*02 01) by BIMAS (Supplementary Table 1) were immunised to HLA-A2 Tgm, and CD4− spleen cells were stimulated in vitro with BM-DCs pulsed with each peptide.

Seven days after the last immunisation, CD4-depleted spleen cells (CD4− spleen cells) from Tgm using CD4 microbeads (Miltenyi Biotec, Auburn, CA, USA) were stimulated in vitro with BM-DCs pulsed with each peptide.

Briefly, splenoyctes from individual mice were stimulated in vitro with 20 µg/ml of each peptide and IFN-γ production was assessed by ELISA after 72 h incubation.