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. Author manuscript; available in PMC: 2025 Sep 9.
Published in final edited form as: Methods Mol Biol. 2023;2652:147–169. doi: 10.1007/978-1-0716-3147-8_8

Fig. 5.

Fig. 5

(a) Tricine gel of purification of AlbM4 peptide (1.5 kDa): lane-1, pellet after lysis; lane-2, supernatant after lysis; lane-3, flow through; lane-4&5, eluted GST-AlbM4; lane-6, cleaved fusion protein; lane-7, pellet after heat treatment; lane-8, supernatant after heat treatment; lane-9, pre-stained ultra-low protein marker. (b) SDS-PAGE of purification of A) S100A13 (11.5 kDa): lane-1, pellet after lysis; lane-2, supernatant after lysis; lane-3, eluted GST-S100A13; lane-4, cleaved GST S100A13; lane-5, pellet after heat treatment; lane-6, supernatant after heat treatment; lane-7, pre-stained protein marker