Sentence examples for lymphocytes were grown from inspiring English sources

Jurkat T lymphocytes were grown in RPMI-1640 supplemented as above.

The lymphocytes were grown in RPMI 1640 medium (GIBCO, 52140; Darmstadt, Germany) supplemented with 10% fetal calf serum (GIBCO) and penicillin/streptomycin (GIBCO).

TK6 cells and lymphocytes were grown in suspension; lymphocyte cultures were treated with the polyvalent mitogen phytohemaglutinin (Sigma /Aldrich; St Louis, MO) as described [ 36].

These lymphocytes were grown, in the presence or absence of kefir, in complete growth medium consisting of RPMI 1640 supplemented with 20% FBS, 2 mM L-glutamine, 100 U/mL penicillin, and 100 μg/mL streptomycin for 24 hours.

Monocyte-depleted ascitic lymphocytes were grown with or without VEGF, cell lysates were prepared using 10 × 10 cells per preparation and subjected to western blotting as described before (Sambrook et al, 1989; Ziogas et al, 2012).

Lymphocytes (Jurkat, CTLL-2, K562) were grown and stably transfected as described in Szabò et al, 2005.

Human Jurkat E6-1 lymphocyTe T cells (ATCC # TIB-152) were grown in RPMI medium supplemented with 10% (v/v) fetal bovine serum (FBS) and maintained in humidified 5%95%% CO2 air at 37°C.

The T-lymphocyte cell lines Sup-T1 and H9 were grown in RPMI 1640 medium.

B-lymphocyte lines prepared from peripheral blood by Epstein-Barr virus (EBV) transformation were grown in supplemented RPMI-1640 medium.

Although the disease is characterized by the presence of autoreactive T lymphocytes, there is growing evidence that B cells play a central role in the pathogenesis of SLE [ 1- 3].

When, however, it is grown in vitro and then used as an antigenic stimulant to cancer lymphocytes, a "cancerlike" result (about 15%) is produced.