pEF1α-E2-Crimson is a mammalian expression vector that constitutively expresses the far-red fluorescent protein E2-Crimson, even after stable integration of the vector into the host cell genome. Stable, constitutive expression of E2-Crimson is driven by the human elongation factor 1 alpha (EF1α) promoter, which allows the protein to be expressed without the transgene silencing associated with CMV promoters. The vector, which lacks an MCS, is designed to be used for cell labeling or as a marker of transfection efficiency.
Overview
Far-red fluorescent protein
E2-Crimson fluorescent protein excitation and emission maxima: 611 and 646 nm, respectively
Map schematic of the plasmid choices that are available carrying the EF1-alpha promoter
Map schematic of the plasmid choices that are available carrying the EF1-alpha promoter. IRES: internal ribosome entry sequence; FP1: fluorescent protein (AcGFP1, DsRed-Monomer, or mCherry); FP2: fluorescent protein (mCherry or ZsGreen1); MCS: multiple cloning site.
pEF1α-E2-Crimson is a mammalian expression vector that constitutively expresses the far-red fluorescent protein E2-Crimson, even after stable integration of the vector into the host cell genome. Stable, constitutive expression of E2-Crimson is driven by the human elongation factor 1 alpha (EF1α) promoter, which allows the protein to be expressed without the transgene silencing associated with CMV promoters. The vector, which lacks an MCS, is designed to be used for cell labeling or as a marker of transfection efficiency.
Overview
Far-red fluorescent protein
E2-Crimson fluorescent protein excitation and emission maxima: 611 and 646 nm, respectively
Map schematic of the plasmid choices that are available carrying the EF1-alpha promoter
Map schematic of the plasmid choices that are available carrying the EF1-alpha promoter. IRES: internal ribosome entry sequence; FP1: fluorescent protein (AcGFP1, DsRed-Monomer, or mCherry); FP2: fluorescent protein (mCherry or ZsGreen1); MCS: multiple cloning site.