(2011) added
BglII and EcoRI restriction sites to forward and reverse primers of Dof1 gene.
The PCR products were digested with BamHI and
BglII and ligated to pTO/IRES2-Venus opened with BamHI.
SLAT2 cDNA was cloned into the
BglII site of pMIG vector, resulting in plasmid pMIG-SLAT2.
The PCR product was cloned to a
BglII site upstream of the flippase recognition target (FRT) in pKD13 (20).
To facilitate cloning into the vector pCAMBIA1301, a restriction enzyme site of PstI was incorporated into a forward primer, whereas a
BglII site was flanked with a reverse primer.
Twenty-one alleles of the IL6 promoter (690 bps, chr7:22732707-22733396) that contained 9 rs1800797 A alleles and 12 rs1800797 G alleles were successfully amplified using primers listed in Supplemental Material, Table S2, from 13 human BEC cultures that were heterozygous for rs1800797 and were directionally cloned into the pGL2-basic luciferase reporter vector (Promega) upstream of the luciferase coding sequence using MluI and
BglII cloning sites according to the manufacturer's instructions.
The amplified fragment was cloned into the NheI and
BglII digested pIRES2-ZsGreen vector for overexpression of WIF-1.
Enzymatic properties and intracellular localization of the novel Trichoderma reesei p-Glucosidase
BGLII (Ce11A).