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
pCB4270BU-amy
Ki Jun Jeong, Department of Chemical and Biomolecular Engineerin
Upstream tips |
Protocol tips |
Downstream tips |
|
The plasmids were purified from E. coli library using GeneAll® Hybrid-QTM Plasmid Rapidprep kit (GeneAll, Seoul, Korea) and transformed into L. citreum CB2567 by electroporation using the following parameters: 25 μF, 1.0 kV, and 400 Ω49. Transformed cells were recovered by incubation on MRS agar plates with 10 mg/L chloramphenicol at 30 °C for 36 h. |
|
Protocol tips |
The plasmids were purified from E. coli library using GeneAll® Hybrid-QTM Plasmid Rapidprep kit (GeneAll, Seoul, Korea) and transformed into L. citreum CB2567 by electroporation using the following parameters: 25 μF, 1.0 kV, and 400 Ω49. Transformed cells were recovered by incubation on MRS agar plates with 10 mg/L chloramphenicol at 30 °C for 36 h. |
pCB4270V4BU-amy
Ki Jun Jeong, Department of Chemical and Biomolecular Engineerin
Upstream tips |
Protocol tips |
Downstream tips |
|
The plasmids were purified from E. coli library using GeneAll® Hybrid-QTM Plasmid Rapidprep kit (GeneAll, Seoul, Korea) and transformed into L. citreum CB2567 by electroporation using the following parameters: 25 μF, 1.0 kV, and 400 Ω49. Transformed cells were recovered by incubation on MRS agar plates with 10 mg/L chloramphenicol at 30 °C for 36 h. |
|
Protocol tips |
The plasmids were purified from E. coli library using GeneAll® Hybrid-QTM Plasmid Rapidprep kit (GeneAll, Seoul, Korea) and transformed into L. citreum CB2567 by electroporation using the following parameters: 25 μF, 1.0 kV, and 400 Ω49. Transformed cells were recovered by incubation on MRS agar plates with 10 mg/L chloramphenicol at 30 °C for 36 h. |
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!