Plasmid History: Constructed by David Kimelman, 6/6/96 XVII p. 98.
Notes for Use: The -3.0kb-siamois promoter was directionally cloned into the KpnI and BglII sites of the luciferase reporter vector pGL3B (Promega) upstream of the luciferase ATG. The -0.8kb promoter construct was generated by digesting the -3.0kb/pGL3B construct with KpnI and at an internal EcoRI site to remove 2.2 kb of intervening sequence, filling in with DNA polymerase I large fragment and religating.
The Kpn site was lost but the R1 site was regenerated in the ligation. The size of the insert is approximate.
Citation: Brannon et al., Gene and Development 11:2359-2370, 1997.
Addgene has sequenced a portion of this plasmid for verification.
Click here for the sequencing
result.
Please acknowledge the principal investigator and cite this article if you use
this plasmid in a publication. Also, please include the text "Addgene plasmid
17157" in your Materials and Methods section.
Plasmid History:
Constructed by David Kimelman, 6/6/96 XVII p. 98.
Notes for Use:
The -3.0kb-siamois promoter was directionally cloned into the KpnI and BglII sites of the luciferase reporter vector pGL3B (Promega) upstream of the luciferase ATG. The -0.8kb promoter construct was generated by digesting the -3.0kb/pGL3B construct with KpnI and at an internal EcoRI site to remove 2.2 kb of intervening sequence, filling in with DNA polymerase I large fragment and religating.
The Kpn site was lost but the R1 site was regenerated in the ligation. The size of the insert is approximate.
Citation: Brannon et al., Gene and Development 11:2359-2370, 1997.