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Fig. 2 | Microbial Cell Factories

Fig. 2

From: Design and validation of recombinant protein standards for quantitative Western blot analysis of cannabinoid CB1 receptor density in cell membranes: an alternative to radioligand binding methods

Fig. 2

Agarose gel electrophoresis of PCR products and transformants. A Agarose gel electrophoresis analysis of PCR amplicons coding for CB1414-472 and CB1414–442 fragments of the cytosolic tail of the human CB1 receptor with expected sizes of 191 and 101 bp, respectively. B BamHI/BsrGI restriction analysis of bacterial clones transformed with pCR-Blunt II-TOPO™ vector containing DNA inserts coding for CB1414–472 and CB1414–442 polypeptides. The restriction maps are consistent with DNA fragments inserted in forward orientation. Expected sizes (bp) of restriction fragments were 3174/493/43 and 3174/403/43 for plasmid with DNA inserts coding for CB1414–472 and CB1414–442, respectively

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