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When the average expression levels of genetically identical clones are compared (e.g. two A2B2 cell lines), the variation between the cell lines is approximately 10 15%.
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clones were compared in a trial established in 1993 at Dalethorpe, Canterbury, New Zealand.
The leaf shapes and transcriptomes of B. pendula 'Dalecarlica' clones were compared with those of B. pendula clones.
The amount of AgaA7 secreted by the clones was compared through activity assay, immuno-blot, and purification via affinity chromatography.
In each case, two samples of XO clones were compared to three samples of normal cells.
Individual clones were compared to consensus sequences as previously described [12].
These clones were compared to wild type and GFP-expressing INS-1 cells for insulin content and release.
A second generation of independent clones was sequenced and the distribution of sequences among the first generation clones was compared to that of the second generation.
When M33 and M34 clones were compared to controls, an increase in SLex with a simultaneous decrease in α2,6-sialic acid was also detected.
In search of FOXM1B-targeted malignancy associated genes, micro-regions of consensus LOH loci shared amongst the 8 malignant clones were compared.
To this end, blood cells from transgenic mice overexpressing PrP specifically on T-cells [18] were used and all clones were compared directly to the previously described monoclonal antibody 6H4 [15] using flow cytometry.
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