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When XEN cells are grown in serum-free medium we again noticed spikes in expression of some markers at some passages but again found no obvious trends in marker expression.
Nevertheless, the absence of resistance associated markers at some homoeologous loci could also be due to our experimental set-up.
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It is reported that the linkage distance between markers varies at some chromosomal regions in different crosses and types of population, but the order of markers remains highly conserved (Antonio et al. [1996]).
There are markers at various sites, including some of the places where flood walls gave way.
We found that despite spikes in some markers at certain passages, that cells grown in standard serum-containing medium are quite stable over seven passages and that there were no obvious trends in marker expression during the duration of this experiment.
We noticed that markers at the end of some LGs were tens of cM distant from adjacent markers.
As a consequence, some markers at the centromeres could not be separated by 184 mapping individuals and co-segregated within recombination blocks.
This map, which is single-population based and thus is not dependent on integration of markers from different populations, may be more accurate in marker order at some positions.
The marker data at some genomic location are a vector of genotypes one for each typed person.
Consequently, the compound appears to be most suitable as a second vascular marker, administered at some time after Hoechst 33342, to detect temporal and spatial fluctuations in tumour perfusion.
The same rational is applicable for some other accession-specific markers at other loci.
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