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. 2012 Jun 20;287(33):27771–27788. doi: 10.1074/jbc.M112.382572

FIGURE 8.

FIGURE 8.

Cx32, SAP97, and CaM coimmunoprecipitation studies using rat Schwannoma cell lysates. A, lysates of RT4-D6P2T cells were incubated with antibodies directed against SAP97 (SAP97 IP) and probed for Cx32 and SAP97. This co-IP was repeated in the presence of EGTA and Ca2+. B, lysates of RT4-D6P2T cells were incubated with antibodies directed against CaM (CaM IP) and probed for Cx32 and CaM. This co-IP was repeated in the presence of EGTA and Ca2+. C, lysates of RT4-D6P2T cells were incubated with antibodies directed against Cx32 (Cx32 IP) in the presence and absence of λ-phosphatase and probed for Cx32, phospho-Ser, and phospho-Tyr. D, lysates of RT4-D6P2T cells were incubated with antibodies directed against IgG (control IP), SAP97 (SAP97 IP), and CaM (CaM IP) and probed for Cx32, SAP97, and CaM. Input is the RT4-D6P2T lysate. Coimmunoprecipitation experiments were performed in triplicate.