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. 2014 Jul 1;5(4):e01312-14. doi: 10.1128/mBio.01312-14

FIG 3 .

FIG 3 

Cellular localization of the AKAP7s in different cell types. 17Cl-1 cells (A) and B6 BMM (B) were infected with chimeric MHV viruses expressing full-length AKAP7, N-terminally truncated AKAP7 (AKAP7ΔNTD), the CD of AKAP7 (AKAP7CD), or its mutant (AKAP7CD H185R) and stained for the expression of ns2 and AKAP7 with monoclonal antibodies against ns2 or against murine AKAP7 CD peptide A. DAPI was used to visualize nuclei. Magnification for panels A and B, ×60. (C) 293T cells expressed AKAP7 or AKAPCD from lentivirus vectors (indicated). Western blot detection of AKAP7 and the AKAP7 CD by immunoblotting with anti-AKAP7 CD antibody (peptide B) and with antibody against β-actin as a loading and transfer control is shown. (D) 293T cell lines expressing AKAP7 or the AKAP7 CD (as in panel C) were stained with a polyclonal antiserum against murine AKAP7 CD peptide A. Nuclei were visualized with DAPI staining. Magnification, ×63.

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