Following electroporation into R26 BirA cells, a cell line that expresses bacterial BirA ligase from the ROSA26 locus, hygromycin resistant clones (200 µg / ml) were expanded for Southern analysis to identify correct targeting events.
Not exact matches
INO - 3112 is injected into a muscle
followed by
electroporation, a technique that uses controlled, millisecond electrical pulses that make it easier for the DNA plasmids to enter muscle cells.
HV cells constitutively expressing the LacZ gene were generated by
electroporation with a vector containing a CAG driven β - Geo cDNA
followed by selection in G418 (150 µg / ml) for 2 wk.
HV cells overexpressing Nanog were generated by
electroporation with a vector containing the Nanog cDNA under the control of a CAG promoter and upstream of IRES Puro cassette
followed by selection in puromycin (2 µg / ml) for 2 wk.
1 - 4 days
following DNA injection and
electroporation, embryonic brains are dissected, sliced, placed on a filter in culture medium and live imaged over night (Baffet et al., Methods Cell Biol., 2015).