Coding
Part:BBa_K1699005:Design
Designed by: Emil Ruvinov Group: iGEM15_BGU_Israel (2015-08-09)
gRNA for dCas9-VP64 targeting synthetic activation promoter pMLPm under U6 promoter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 250
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
gRNA in SaCas9 scaffold under U6 promoter. Designed to complement 3 sites on MLP synthetic promoter.
Cloned into pSBC13 using EcoRI and PstI restriction sites.
F. tagtcatggcggccgcgtcgacG
R. actgacatgcggccgcttaattaaC
Source
gMLP from IDT de-novo synthesis. Cloning with U6 to pSBC13 was done by team BGU 2015.