sample review
- pMD2.G was used for cell transfection analysis, in order to study the mechanism by which Cry1/2 protect genomic integrity.
- psPAX was used for cell transfection analysis, in order to study the mechanism by which Cry1/2 protect genomic integrity.
- pLenti-lox-GFP shRNA p19-2 was used for cell transfection analysis, in order to study the mechanism by which Cry1/2 protect genomic integrity.
- pLKO.1 sh_scramble was used for cell transfection analysis, in order to study the mechanism by which Cry1/2 protect genomic integrity.
- pCl-neo Flag HAUSP was used for cell transfection analysis, in order to study the mechanism by which Cry1/2 protect genomic integrity.
- Expression plasmid was used for confocal microscopy analysis in order to study the effects of aneuploidy on chromosome mis-segregation and cytokinesis failure.
- pRL-SV40P was used for luciferase reporter assay in order to study the effect of Ataxia-telangiectasia mutated (ATM) depletion on cell migration and invasion in a cancer-promoting process.
- pNANOG-Luc was used for luciferase reporter assay in order to study the effect of Ataxia-telangiectasia mutated (ATM) depletion on cell migration and invasion in a cancer-promoting process.
- Addgene pCMV-SEAP was used to perform cell transfection in order to study study the regulation mechanism of protein quality control by UBE4B and LSD1.
- Addgene p53 shRNA plasmid pLVTH-sip53 was used to perform cell transfection in order to study study the regulation mechanism of protein quality control by UBE4B and LSD1.
- Addgene pLVTHM was used to perform DNA cloning in order to study the regulation of FGF14 on resurgent sodium current in mouse cerebellar Purkinje neurons.