In all cases, purity of the plasma cells was higher than 90%, as assessed by morphology or CD138 staining.
In all cases, purity and quality of DNA was assessed using a nanodrop spectrophotometer and gel electrophoresis analysis.
Here, it is imperative that every cell is isolated from the sample, but in these cases, purity is not as important.
In this case, high purity La1−xCaxAl1−yNiyO3 (x = 0, 0.1; y = 0.1, 0.2, 0.3) perovskites were chosen, prepared by the citrate method and evaluated in the ethanol steam reforming reaction.
Our modeling has shown that for low molar composition x, the concentration of holes in the well is high in a wide range of electron concentrations; in this case, the purity of samples does not significantly influence the electron mobility.
Still, even in this worst case, P34 purity was sufficiently high.
After thawing, CLL cells were enriched, in case CD19/CD5 purity was below 90%, via negative depletion using α-CD3 (CLB-T3/4,1,nr70,1x1), α-CD14 (CLB-mon/1,nr143,8G3) and α-CD16 (CLB-FCRgran1,nr142,5D2) (CLB, Amsterdam, the Netherlands) as described.
In all the cases, high purity MTBE has been obtained.
In all the cases, high purity MTBE has been obtained as a product.
In all cases cell purity was over 90%.
