A nos promoter drives expression of phiC31:int integrase, which is tagged with a nuclear localization signal (Tag:NLS(SV40-largeT)). nos 3'UTR sequences are also present.
Generated by phiC31\int-mediated integration of p3xP3-EGFP.nos-int.NLS.attB into a target "landing site" insertion of the M{3xP3-RFP.attP} construct.
The resulting inserted construct consists of a P1\loxP site, followed by a Disc\RFP3xP3.PB marker, followed by another P1\loxP site, followed by a Avic\GFPE.3xP3 marker, followed by another P1\loxP site, followed by phiC31\intnos.T:SV40\nls2, which provides the integrase source. The presence of the P1\loxP sites mean that it is possible to eliminate the Disc\RFP3xP3.PB and Avic\GFPE.3xP3 markers by cre-mediated recombination.
Generated by phiC31\int-mediated integration of p3xP3-EGFP.nos-int.NLS.attB into a target "landing site" insertion of the M{3xP3-RFP.attP} construct.
The resulting inserted construct consists of a P1\loxP site, followed by a Disc\RFP3xP3.PB marker, followed by another P1\loxP site, followed by a Avic\GFPE.3xP3 marker, followed by another P1\loxP site, followed by phiC31\intnos.T:SV40\nls2, which provides the integrase source. The presence of the P1\loxP sites mean that it is possible to eliminate the Disc\RFP3xP3.PB and Avic\GFPE.3xP3 markers by cre-mediated recombination.