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The independently generated T0 generation transgenic lines were analysed by PCR.
The changes in cell cycle and gene expression of cell lines were analysed by flow cytometry and qRT-PCR, respectively.
Due to this assumption the reflected lines were analysed by structural crystallography method ('Powder method').
After selection in gancyclovir, resistant cell lines were analysed by PCR to ensure the selectable marker had been removed.
Resistant cell lines were analysed by PCR to ensure that the selectable marker gene had been removed (data not shown).
After 14 days, these lines were analysed by tetramer staining.
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Population structure of the 192 germplasm lines was analysed by Bayesian based approach.
The IgG binding to tumour cell lines was analysed by FACS (figure 11).
Correlation between expression of both antigens in cell lines was analysed by immunoblot and flow cytometry.
Desmocollin 3 expression in CRC cell lines was analysed by RT PCR and western blotting.
The expression of Dkk-1 in human breast cancer cell lines was analysed by RT PCR.
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