
Polyribosome sedimentation velocity centrifugation can be used to identify differential regulation of the translation of mRNAs. However, ultracentrifugation presents practical limitations on the number of sedimentation velocity gradients that can be run simultaneously. A method for sedimentation velocity analysis of polyribosomes is presented that is based on low-speed centrifugation of sucrose gradients prepared in deep 96-well plates, the advantage of which is that hundreds of polyribosome fractionations can be performed simultaneously in a tabletop centrifuge.
Reverse Transcriptase Polymerase Chain Reaction, Cell Fractionation, Gene Expression Regulation, Cell Line, Tumor, Polyribosomes, Protein Biosynthesis, Centrifugation, Density Gradient, Humans, Puromycin, RNA, Messenger, Ultracentrifugation
Reverse Transcriptase Polymerase Chain Reaction, Cell Fractionation, Gene Expression Regulation, Cell Line, Tumor, Polyribosomes, Protein Biosynthesis, Centrifugation, Density Gradient, Humans, Puromycin, RNA, Messenger, Ultracentrifugation
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 11 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
