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The analysis shown in Figure 2A (upper panel) indicates increased amounts of WT GFP SRY-HMG in the nuclear fraction compared with the cytoplasmic fraction, with clearly increased amounts of GFP SRY in the cytoplasmic fractions for all of the mutant proteins.
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That indicates increased marketing efficiency.
Change indicates increase or decrease in the percentage.
Detection of IGF-1R was significantly increased in the anti-InsRα immunoprecipitated supernatant from InsR silenced cells, indicating increased formation of IGF-1R homodimers (middle panel, Figure 6B).
When AR was knocked down, the amount of AR protein was reduced (lower panel, lanes 3 and 4), coupled with a decreased growth rate of LNCaP cells overexpressing BCAS2, and of the GFP control cells (upper panel), indicating that the increased growth rate associated with BCAS2 may be connected to the increased expression of AR.
The red panel indicates the transcription level of gene increased over twofold; the green panel indicates the transcription level of gene decreased over twofold.
The red panel indicates that the transcription level of gene increased over twofold; the green panel indicates the transcription level of gene decreased over twofold.
Detection of unaltered IRP1 expression (Fig. 3E, upper panel) but increased IRP2 expression by Western analysis (Fig. 3E, lower panel) indicates an iron-depleted condition in LD-infected host macrophages.
Each arrow in each panel indicates the frequency of fUHR.
Box-shaped panel indicates the proteins in mesophyll cell (a).
The lowest panel indicates control PCR amplifying tubulin genetic region.
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