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(c) The established cell lines were analyzed for live cell imaging for fluorescent signals.
Non-SA treated calli of these lines were analyzed first by PCR for spontaneous excision events.
METHODS: Five metastatic prostate cancer cell lines were analyzed for p16 gene structure and its expression by Southern and Northern blot analyses.
Expression patterns of CHIT2, PR10, and Betv1 in OsWRKY11-kd lines were analyzed using RT-PCR with gene-specific primers.
Five MPNST cell lines were analyzed.
For each reporter construct, three independent transgenic lines were analyzed.
Three independent stable lines were analyzed by confocal microscopy.
All HSP90-RNAi and HSP90-TDNA lines were analyzed, along with the hsp90.2-3 hsp90.2-3
FIB and TER lines were analyzed at the passages listed in Table 1.
No pronounced flowering phenotype was detected when 35S::DWF4 lines were analyzed (Fig 3, 4).
In a second set of experiments, TH cell lines were analyzed for T cell receptor Vβ chain (TCR-Vβ) expression.
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