The effect of the filing tool design on the morphology and hydrogen storage properties of Mg chips was evaluated.
Neo-vasculogenesis within the LAB chips was evaluated using anti-CD31 (PECAM-1) (Santa Cruz), anti-von-Willebrand (domain 1 and 2) and anti- ACE (kind gifts of Dr Massimo Ragni, School of Medicine, University Federicoo II', Naples Italy) all mouse anti-human.
The bonding quality of the chips was evaluated by employing SEM, shear strength testing procedure and electric current measurement at different applied voltages.
Magnetic fields in pores and the force effect of these fields on magnetic particles and the magnetization properties of packed beds composed of ferromagnetic spheres and metal chips are evaluated.
At total of 209 exonic SNPs with available genotype data from the exome chip were evaluated for association with clinical CVD, subclinical CVD, and CVD risk factors.
The chip was evaluated via absorbance measurements, polymerase chain reaction (PCR), and gel electrophoresis.
The performance of the chip is evaluated using an electrolyte and a well-established confluent cell line.
As this array consists of non-discrete tiled regions, the association of log2 ratios from MYCN ChIP-chip and MeDIP-chip was evaluated using Pearson's correlation and its corresponding p-value.
The ChIP was evaluated by qPCR using "platinum SYBR Green qPCR SuperMix-UDG" from Invitrogen.
