ACQUITY UPLC Col. In-Line Filt

【精华】vol 687 Chapter 3 采用Splinkerette-PCR技术对前病毒基因组插入位点进行分离

of more sophisticatedand streamlined protocols that better accommodate theemerging large-scale insertion site mapping efforts. In line with thistrend, a Web-based automated analysis and mapping of insertionalmutagenesis sequence data has recently become available (29

Growth, Maintenance and Transfection of Suspension Adapted 293-EBNA cells

Procedure I. INTRODUCTION The 293 EBNA cell line is established from primary embryonal human kidney cells transformed with sheared human adenovirus type 5 DNA and Epstein-Barr virus nuclear antigen 1, allowing episomal amplification

Isolate It All：siRNA • miRNA • Total RNA • Native Protein

inactivation of cellular ribonucleases. After a rapid extraction with Acid-Phenol:Chloroform (provided with the kit), total RNA was then purified from the mixture using an RNA-binding glass fiber filter (GFF) and optimized binding and wash buffers