Sentence examples for microscopy experiments showing from inspiring English sources

(E ) Confocal microscopy experiments showing that HTT proteins are enriched in the perinuclear and co-localize with the endoplasmic reticulum (ER) marker calreticulin upon treatment of Rp-cAMP or 8-pCpt-2′-O-Me-cAMP (8-pCpt-cAMP for short).

Optical microscopy experiments showed that both peptides induced pore opening and the dimer eventually caused the vesicles to burst.

Confocal laser scanning microscopy experiments showed that ARH could be used to detect Fe3+ in living cells.

Confocal laser scanning microscopy experiments showed that rhodamine B-2-aminobutenedioate can be applied to detect acidic pH variations in living cells with a turn-on signal.

The results of the fluorescence microscopy experiments show that the encrypted polymers direct vesicular escape and efficiently deliver oligonucleotides and macromolecules into the cytoplasm of hepatocytes.

Small angle X-ray scattering patterns of the materials and transmission electronic microscopy experiments show that the mesoporous network (mesopore size around 9 nm) adopts a hexagonal arrangement.

Small angle light scattering and confocal microscopy experiments show that the mechanism of phase separation is similar to spinodal decomposition, even in the presence of a rapid gelation.

Fluorescent microscopy experiments showed that the second and third generations are the most efficient for cellular uptake with the second generation having the synthetic advantage.

In the first part, scanning electron microscopy experiments show that the two-phases composition of the semi-IPN NBR/PEDOT obtained notably the localization of PEDOT inside the NBR matrix.

In situ immuno-electron microscopy experiments showed the minor subunit (FimH) mediating pilus adhesion to bladder epithelial cells to be the distal protein of the pilus tip, which had a spring-like appearance at higher magnification.

Confocal immunofluorescence microscopy experiments showed extensive co-localization of the HER2 receptor and ZHER2 00477-KDEL in the ER, whereas the use of a KDEL-extended control affibody molecule resulted in distinct and separate signals from cell surface-localiZHER2 00477-KDELr and ER-localined affibody prothen.