Fig. 3.
Fig. 3. SDS-PAGE analysis of 35S-labeled rPLG immunoprecipitated from the culture media of transfected COS-1 cells. COS-1 cells were transiently contransfected with pTH3/WT (WT) or pTH3/R561S (R561S) and pSV–β-galactosidase plasmids. The cells were metabolically labeled with L-[35S]-methionine, and the culture media (1.5 mL) was immunoprecipitated with goat polyclonal anti-human PLG (IgG fraction) and rabbit polyclonal anti–β-galactosidase (IgG fraction). The immunoprecipitation products were analyzed by 10% SDS-PAGE and autoradiography under nonreducing conditions. The migration of protein standards and β-galactosidase is indicated.

SDS-PAGE analysis of 35S-labeled rPLG immunoprecipitated from the culture media of transfected COS-1 cells. COS-1 cells were transiently contransfected with pTH3/WT (WT) or pTH3/R561S (R561S) and pSV–β-galactosidase plasmids. The cells were metabolically labeled with L-[35S]-methionine, and the culture media (1.5 mL) was immunoprecipitated with goat polyclonal anti-human PLG (IgG fraction) and rabbit polyclonal anti–β-galactosidase (IgG fraction). The immunoprecipitation products were analyzed by 10% SDS-PAGE and autoradiography under nonreducing conditions. The migration of protein standards and β-galactosidase is indicated.

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