Figure 1
Figure 1. Physical interactions between Fech with either Mfrn1 or Abcb10 proteins are confirmed in endogenous MEL cells and transfected heterologous cells. (A) IP/Western blot analysis of interactions of endogenous Fech with Mfrn1 and Abcb10 in differentiated MEL cells stably expressing empty vector, engineered Mfrn1-FLAG, or Abcb10-FLAG. (B) IP/Western blot analysis of interactions of heterologous Fech with Mfrn1 and Abcb10 from transiently cotransfected HEK293 cells with control vector, Mfrn1-FLAG, or Abcb10-FLAG. Protein input lysate is shown on the respective left columns. Fech is selectively copurified in the presence of Mfrn1 or Abcb10.

Physical interactions between Fech with either Mfrn1 or Abcb10 proteins are confirmed in endogenous MEL cells and transfected heterologous cells. (A) IP/Western blot analysis of interactions of endogenous Fech with Mfrn1 and Abcb10 in differentiated MEL cells stably expressing empty vector, engineered Mfrn1-FLAG, or Abcb10-FLAG. (B) IP/Western blot analysis of interactions of heterologous Fech with Mfrn1 and Abcb10 from transiently cotransfected HEK293 cells with control vector, Mfrn1-FLAG, or Abcb10-FLAG. Protein input lysate is shown on the respective left columns. Fech is selectively copurified in the presence of Mfrn1 or Abcb10.

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