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pET44a-CrtY
Young Tae Kim, Department of Microbiology, Pukyong National Univ
Upstream tips |
Protocol tips |
Downstream tips |
The gene product of the carotenoid biosynthesis genes was expressed by subcloning crtY genes into the expression vector, pET44-a(+), which allows expression of a recombinant protein with a C-terminal fusion His-tag. |
The expression plasmids were individually constructed under the control of the T7 promoter, and resulted in a pET44a(+)-CrtY plasmid (Fig. 1). This plasmid was transformed into the E. coli BL21(DE3) codon plus strain. The overexpression of crtY was induced by adding
isopropyl-β-D-thiogalactopyranoside (IPTG) to a final concentration of 0.05 mM at a cell density of OD600 = 0.5. The recombinant protein was overexpressed by adding IPTG and incubating at 25o C. |
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Upstream tips |
The gene product of the carotenoid biosynthesis genes was expressed by subcloning crtY genes into the expression vector, pET44-a(+), which allows expression of a recombinant protein with a C-terminal fusion His-tag. |
Protocol tips |
The expression plasmids were individually constructed under the control of the T7 promoter, and resulted in a pET44a(+)-CrtY plasmid (Fig. 1). This plasmid was transformed into the E. coli BL21(DE3) codon plus strain. The overexpression of crtY was induced by adding
isopropyl-β-D-thiogalactopyranoside (IPTG) to a final concentration of 0.05 mM at a cell density of OD600 = 0.5. The recombinant protein was overexpressed by adding IPTG and incubating at 25o C. |
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