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Figure 7 shows that PKC phosphorylation or leucine zipper deletion increases AFAp-110 ability to cross link actin filaments by incubating them with actin filaments (A) and incubating them with rhodamine-phalloidin-labeled actin filaments.

Figure 3 shows rAFAP cross links actin filaments by incubating them with rhodamine-phalloidin-labeled actin filaments.

Figure 2 shows that rAFAP-110 cross links actin through carboxyl terminal region by using a low-speed cosedimentation assay (A), and centrifugation of cross linked actin filaments versus free rAFAP-110 (B).

Figure 1 shows that rAFAP-110 bind to actin filaments directly by using gel electrophoresis, EM negative staining, and centrifugation.

Analysis from article. See Figure 4. Shows the multiple sequence alignment of the G domain which is part of he SHBG family

Analysis of Paper. See Figure 2. Shows images of the human SHBG steroid-binding site

Analysis of Paper. See Figure 1(b). Shows the Amino acid sequences determined by peptides. Those generated from SHBG are underlined

See Figure 2. It shows the amino acid sequence of SHBG gotten from the sequence of its cDNA.

Analysis of Paper. See Figure 1. Gel Electrophoresis

Analysis from FIgure 1 Northern blotting, and Figure 3 Sequence Alignment

Analysis of Sequence ALignment, Figure 2

Sequence analysis

Northern and Sequence Analyses

Analysis of data using Northern blotting, sequence alignment and expression vectors

Figure 1 shows the analysis of a putative nuclear localization signal of huntingtin in an in vivo assay of human HeLa epithelial cells. It does not contain a classic nuclear localization signal.