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Description
Cell 89, 28796 (1997)
Los resultados varan dependiendo de su edad, estado de salud, mtodo de administracin y la preocupacin especfica siendo abordada
To analyze the endogenous complex formation in vivo between MAGE-G1 and VIME during neuronal differentiation, we carried out endogenous immunoprecipitation in P19 cells after 6-day treatment with RA
The proteins were visualized by exposure machine (GE, Amersham Imager 680) using Pierce ECL Plus Western Blotting Substrate (Thermo Fisher Scientific, 32132) and the protein bands were quantitatively analyzed with ImageJ software
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