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Figure 1d showed that DPP10 facilitated cell membrane surface expression of Kv4.2 protein through in situ hybridization.

accession #:AY172661

figure 1c shows that DPPX (DPP6) promoted a robust trafficking of Kv4.2 to the plasma membrane.

accession #:M76427

Table 1

Results section 3.5 and Figure 5 detail that nucleus localization occurs because of a bipartite NLS in the protein. Epifluorescence microscopy was used to determine the localization pattern.

Section of the text labeled "Biochemical Characterization of Lbh protein" refers to N and C terminus labeling using an antibody to detect localization of the Lbh protein in the nucleus. (figure 2b)

Figure 1c showed Western Blot Analysis was used to confirm localization of the MCC protein to the cytoplasm.

Figure 1c showed the use of Western Blot Analysis to confirm MCC protein localization in the nucleus of cells.

Figure 4C and 4D shows that MCC regulates the cell cycle by suppressing the DNA-binding activity of β-catenin/TCF/LEF in the nucleus through Western Blot Analysis. This is also confirmed in the section of the text "MCC interacts with β-catenin, blocks β-catenin/TCF/LEF DNA binding, and can affect endogenous β-catenin localization/levels".

The section of the text "MCC interacts with β-catenin, blocks β-catenin/TCF/LEF DNA binding, and can affect endogenous β-catenin localization/levels" confirms that MCC relocalizes the β-catenin to the cytoplasm. The results are further confirmed through Western Blot Analysis in Figure 4.

Immunofluorescence was used and confirmed in Figure 6A/B to show that MCC is responsible for the suppression of basal cell growth.

Figure 2.a/b show evidence of %Pepsin activity severely decreased between pH of 2-4.5. Supported text for the experiment is listed under "Inhibitory Activities of Uterine Secretions" with standard assay.

figure 5 shows through confocal microscopy, localization of QPP (DPP2) to the vesicles.

figure 1b shows through immunoelectron microscopy, that ZmpB localizes to the cell surface.

Figure 7 shows endothelial cell apoptosis caused by halysase through fluorescence.

Figure 6 shows that DREAM represses basal prodynorphin expression in the spinal chord.

figures 4 and 5 show that AUX1 causes root hair development over time through microscopy.

figure 3 shows that AUX1 restores gravitropic root growth.

figure 4 shows that axr2 has an agravitropic affect on root growth through a rescue experiment.

figure 4 shows that axr3 has an agravitropic effect on root growth.

Figure 5 shows that NUANCE localizes to the nucleus through immunolabeling.

Figure 5 shows that NUANCE can localize to the cytoplasm through immunolabeling.