Cloning and Expression of the Intracellular Cytoplasmic Domain of Rat Notch 1 Receptor
Weilin Jin, Baisong Liao, Ju Gong
Abstract
Weilin Jin, Baisong Liao, Ju Gong
Abstract
The cloned NICD fragment was confirmed by sequencing and then subcloned into glutathione-S-transferase (GST) fusion protein expression vector pGEX-KG. The GST-NICD fusion proteins were expressed in E. coli JM109 after inducing by IPTG. The fusion proteins were purified by affinity chromatography on glutathione Sepharose 4B.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The cloned NICD fragment was confirmed by sequencing and then subcloned into glutathione-S-transferase (GST) fusion protein expression vector pGEX-KG. The GST-NICD fusion proteins were expressed in E. coli JM109 after inducing by IPTG. The fusion proteins were purified by affinity chromatography on glutathione Sepharose 4B.
Key concepts: Fusion protein, lac operon, Affinity chromatography, Molecular biology, Cloning (programming), Sepharose, Glutathione S-transferase, Glutathione