Sentence examples for blot analysis was employed from inspiring English sources

Western blot analysis was employed to quantify total numbers of hippocampal NR2A and NR2B.

Western blot analysis was employed to evaluate levels of AMPK, mTOR, raptor, Beclin-1, p62 and LC3-II.

The same anti VILIP-1 antibody used in Western blot analysis was employed as primary antibody at 1/500 and 1/1000 dilutions.

Western blot analysis was employed to quantify GFP expression.

Western blot analysis was employed to determine the protein levels of two autophagy markers, Light Chain 3 (LC3) and beclin‐1.

A pull-down assay with glutathione S-transferase (GST -agarose beads followed by Western blot analysis was employed to confirm microtubule S-GST -agaroseation. Immunofluorescence microscopy using a mouse monoclonal anti-α-tubeads-followed used to study the effect of the S-glutathionylation on microtubyle function; mainly polymerization and depolymerization.

Quantitative real-time polymerase chain reaction arrays and Western blot analysis were employed to identify the cell-cycle control- and apoptosis-related genes regulated by CENP-A.

SDS-PAGE and Western blot analysis were employed to determine the enrichment of serum.

RT Q-PCR and Western blot analysis were employed to investigate the activities of AMPK, FOXM1 and AKT/FOXO3a signaling.

Spectrofluorimetry, circular dichroism (CD) studies, in vitro histone acetyl transferase (HAT) assay and western blot analysis were employed as experimental tools.

Real-Time PCR and Western blot analysis were employed to validate the changes in expression of relevant genes including the protein levels of C3 which is a component of the complement cascade.