Total protein analysis as a reliable loading control for quantitative fluorescent Western blotting.

In addition to their direct and indirect roles in the control of hepatitis B virus gene expression and replication, miRNAs are involved in immune response by controlling the

Total cell extracts were blotted with antibodies against CXCR7 (42 kDa), CXCR4 (42 kDa) or b -actin (42 kDa), as a control for equal sample loading, and developed with the ECL

(B) SAP expression was determined by quantitative western blot using total protein extracts from epimastigotes and metacyclic trypomastigotes (15 m g protein/lane) reacted with

Relative levels of dysbindin-1A, -1B, and 1C in synaptosomal fractions of the pSTG from schizophrenia cases compared to their matched normal controls based on Western blotting

Western blot confirmed the expression of TG-1, TG-2, TG-3 and TG-5 proteins in mouse and human scleral fibroblasts.. ß-tubulin was used as a

In this study we used a 2D-LC MS/MS iTRAQ proteomic analysis, western blotting, and pathway analysis to analyze changes in protein expression 24-hours after rt-PA administration in

a) Phenotypic analysis of these glycosidic antigens by Dot Blotting to analyze the expression of E-SL in matched normal and tumor LC tissues. b) Expression analysis

We observed that the Poisson's ratio calculated for both loading and unloading, presented higher values than the experimental values, with the increase of