Sentence examples for measured cell surface from inspiring English sources

We measured cell surface β1 integrin abundance in non-permeabilized DDR1 control, DDR1 over-expressing cells, DDR1 wild type and DDR1 knock down cells by immunostaining and flow cytometry.

To assess whether the relative abundance of TRAIL receptors on the cell surface accounted for differences in sensitivity to TRAIL-induced apoptosis, we measured cell surface expression of TRAIL-R1, -R2, -R3 and -R4 by flow cytometry.

> -wrap-foot> The measured cell surface was used to calculate the average radius of the cells.

Here we have investigated the portion and activation status of several leukocyte subpopulations and measured cell surface S100A8/A9 on these cells, corresponding S100A8 and S100A9 mRNA expression as well as serum levels of S100A8/A9 in healthy controls and SLE patients to learn more about the role of these proteins in SLE.

To determine whether SUMOylation of sPRDM16 was involved in differentiation of AML cells, we treated cells stably transfected with Lenti-Vector, sPRDM16 WT and sPRDM16 K568R with 3 nM PMA for 24 h and measured cell surface expression of the monocytic maturation marker CD11b by flow cytometry.

Polymorphonuclear neutrophil activation was analyzed by measuring cell surface and soluble cell adhesion molecule expressions.

Immune responses were quantified by measuring cell surface marker expression with flow-cytometric analysis and mRNA levels with quantitative reverse transcriptase-polymerase chain reactions in whole blood before and after exposure.

We assessed class-switching of atypical MBCs by measuring cell surface expression of IgG by flow cytometry (Fig. 4).

Using fluorescently labelled anti-ErbB2 or anti-EGFR extracellular antibodies allowed us to measure cell surface ErbB2 and EGFR levels following POH1 knockdown by FACS analysis (Figure 7A,B).

We tested the effects of over expression of RACK1 in transiently expressing HEK cells by co-transfecting Flag-M2 with either PCDNA3.1 or RACK1 into HEK cells and used the membrane-impermeable antagonist ([3H]NMS) binding to measure cell surface receptors after 5, 15, 30 and 60 minutes of carbachol stimulation (Fig. 2B).

To measure cell surface PTPRZ1 levels in sh Z1-transduced SCLC cells, we used flow cytometry (FACS).