No discussions found
Start your discussion
Share your thoughts or question with experts in your field
Start a discussion
Found 2 matching solutions for this experiment
CAPNS1/pACpET
Shoji Hata,Calpain Project, Department of Advanced Science for B
Upstream tips |
Protocol tips |
Downstream tips |
|
CAPN1/pET or CAPN1:C115S/pET was co‐transformed into E. coli strain SoluBL21 (Genlantis) with CAPNS1/pACpET or CAPNS1ΔGR/pACpET, and the transformants were stored as frozen glycerol stocks at −80 °C. For protein expression and purification, the frozen transformants were precultured at 27 °C overnight, in 50 mL LB medium containing 100 μg/mL ampicillin and 50 μg/mL kanamycin (LB+Amp+Kn), and the cultures were then diluted into 1 L LB+Amp+Kn, and grown at 27 °C with vigorous shaking until A600 reached 0.4–0.5. The recombinant protein expression was induced by adding 1 mm isopropyl thiogalactoside (IPTG), followed by a 20‐h incubation at 24 °C, with vigorous shaking. |
|
Protocol tips |
CAPN1/pET or CAPN1:C115S/pET was co‐transformed into E. coli strain SoluBL21 (Genlantis) with CAPNS1/pACpET or CAPNS1ΔGR/pACpET, and the transformants were stored as frozen glycerol stocks at −80 °C. For protein expression and purification, the frozen transformants were precultured at 27 °C overnight, in 50 mL LB medium containing 100 μg/mL ampicillin and 50 μg/mL kanamycin (LB+Amp+Kn), and the cultures were then diluted into 1 L LB+Amp+Kn, and grown at 27 °C with vigorous shaking until A600 reached 0.4–0.5. The recombinant protein expression was induced by adding 1 mm isopropyl thiogalactoside (IPTG), followed by a 20‐h incubation at 24 °C, with vigorous shaking. |
CAPNS1ΔGR/pACpET
Shoji Hata,Calpain Project, Department of Advanced Science for B
Upstream tips |
Protocol tips |
Downstream tips |
|
CAPN1/pET or CAPN1:C115S/pET was co‐transformed into E. coli strain SoluBL21 (Genlantis) with CAPNS1/pACpET or CAPNS1ΔGR/pACpET, and the transformants were stored as frozen glycerol stocks at −80 °C. For protein expression and purification, the frozen transformants were precultured at 27 °C overnight, in 50 mL LB medium containing 100 μg/mL ampicillin and 50 μg/mL kanamycin (LB+Amp+Kn), and the cultures were then diluted into 1 L LB+Amp+Kn, and grown at 27 °C with vigorous shaking until A600 reached 0.4–0.5. The recombinant protein expression was induced by adding 1 mm isopropyl thiogalactoside (IPTG), followed by a 20‐h incubation at 24 °C, with vigorous shaking. |
|
Protocol tips |
CAPN1/pET or CAPN1:C115S/pET was co‐transformed into E. coli strain SoluBL21 (Genlantis) with CAPNS1/pACpET or CAPNS1ΔGR/pACpET, and the transformants were stored as frozen glycerol stocks at −80 °C. For protein expression and purification, the frozen transformants were precultured at 27 °C overnight, in 50 mL LB medium containing 100 μg/mL ampicillin and 50 μg/mL kanamycin (LB+Amp+Kn), and the cultures were then diluted into 1 L LB+Amp+Kn, and grown at 27 °C with vigorous shaking until A600 reached 0.4–0.5. The recombinant protein expression was induced by adding 1 mm isopropyl thiogalactoside (IPTG), followed by a 20‐h incubation at 24 °C, with vigorous shaking. |
Can't find the product you've used to perform this experiment? It would be great if you can help us by
Adding a product!