Figure 2.
HEK293 cell extracts overexpressing LRRK2[Y1699C] and the indicated HA-tagged Rab protein were treated ±150 nM MLi-2 for 90 min and then lysed. The cell lysates were immunoblotted with the indicated sheep (A) and rabbit (B) affinity-purified phospho-specific polyclonal antibodies (all at 1 µg/ml antibody — for only sheep polyclonal antibodies, we also included 10 µg/ml dephospho-peptide antigen). Ten micrograms of whole cell lysate were loaded per lane for the sheep polyclonal antibodies (A) and 1 µg of cell lysate per lane for the rabbit polyclonal antibodies (B). Immunoblots developed with ECL.
Cross-reactivity of the polyclonal sheep and rabbit phospho-Rab protein antibodies.

HEK293 cell extracts overexpressing LRRK2[Y1699C] and the indicated HA-tagged Rab protein were treated ±150 nM MLi-2 for 90 min and then lysed. The cell lysates were immunoblotted with the indicated sheep (A) and rabbit (B) affinity-purified phospho-specific polyclonal antibodies (all at 1 µg/ml antibody — for only sheep polyclonal antibodies, we also included 10 µg/ml dephospho-peptide antigen). Ten micrograms of whole cell lysate were loaded per lane for the sheep polyclonal antibodies (A) and 1 µg of cell lysate per lane for the rabbit polyclonal antibodies (B). Immunoblots developed with ECL.

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