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Finally, a full-length cDNA clone containing an engineered SacII site that served as a genetic marker was obtained.
The activation of Smad, an osteoblastic differentiation marker, was obtained in the cell culture gel of self-assembled OPDA; therefore, the intracellular signal transduction for osteogenesis was performed like an OPD peptide.
Dig-labeled RNA size marker was obtained from Roche.
Polymorphism level of 2.4 alleles per marker was obtained.
Precision Plus Pre-stained molecular weight marker was obtained from Bio-Rad.
The 600 bp DNA ladder marker was obtained from Tianze Genetic Engineering Co. Ltd. (China).
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Strains containing multiple disruptions with the same auxotrophic marker were obtained from genetic crosses and confirmed by PCR.
The +/gcs1 plants were crossed with the transgenic Arabidopsis expressing HTR10-RFP (sperm nucleus marker), and the F1 +/gcs1 plants hemizygously expressing the marker were obtained.
Cutoff points for each tumor marker were obtained with ROC analysis.
Sequence statistics for specified regions of each marker were obtained utilizing SeqState [ 75].
PCR product lengths for each marker were obtained by using Genemarker software.
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