Positions of these markers were determined through alignment on the physical map of lettuce19.
Three pro-inflammatory and 3 hypoxia markers were determined in the serum.
However, no significant correlations between lipoprotein levels and levels of inflammation markers were determined.
Tissue architecture and expression of markers were determined by histochemical and immunohistochemical techniques.
In the serum and liver, the level of nonenzymatic antioxidants and lipid and protein oxidation markers were determined.
Maintenance of a confluent cell layer and deposition of basement membrane markers were determined with immunohistochemical labeling.
Terminally, acetylcholinesterase (AChE) activity and the levels of oxido-nitrosative stress markers were determined in cortical and hippocampal brain regions of rats.
Of the 225 detected microsatellite loci, 108 loci were suitable for primer design, and 12 of the microsatellite markers were determined to be highly polymorphic, amplifying on average 5.7 alleles per locus.
The foreground (particle) and background markers were determined by the coarse estimation step.
The marker order and the genetic distance between every two adjacent markers were determined in the target region on chromosome 5.
Physical positions of SSR markers were determined by one of two methods depending on which genome had been used for SSR marker design.
