Procedure
By simply mixing E. coli extract, master mix and template DNA (prepared by PCR or cloning), your
target protein will be expressed in a water bath at 30C. And the target protein is purified using Ni-NTA
magnetic beads and buffer provided in the kit.
When synthesized protein is not detectable on SDS-PAGE with coomassie blue staining, you can use western blot or fluorescence for it detection.
Experimental results
Protein Synthesis using AccuRapid™ Protein Synthesis Kit
Expression sample |
Purification sample |
|
|
Figure 1. SDS-PAGE data of various proteins synthesized from various templates
M; AccuLadder™ Protein Size Marker (Broad)
1; CalmL3 (17.5 kDa), 2; DUSP 3 (22 kDa), 3; CAT (24 kDa), 4; AcGFP (29 kDa),
5; ERFP (31 kDa), 6; EF-Ts (34 kDa), 7; VF (45 kDa), 8; BM3 (117 kDa)