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. 2017 Feb 6;12(2):e0171328. doi: 10.1371/journal.pone.0171328

Fig 4. Evaluation of disulfide bond(s) location in the SRPK1 molecule.

Fig 4

(A) Lysates from 293T cells overexpressing FLAG-SRPK1 or FLAG-SRPK1Δspacer were analyzed by SDS-PAGE, under non-reducing or reducing conditions, and Western blotting. SRPK1 was detected using the M5 anti-FLAG monoclonal antibody. (B) Amino acid sequence of SRPK1. The two catalytic domains are highlighted by grey shadows. All cysteines are marked in red; underlined cysteines were mutated to alanine or glycine.