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A subgenomic promoter is a promoter added to a virus for a specific heterologous gene, resulting in the formation of mRNA for that gene alone. Many positive-sense RNA viruses produce these subgenomic mRNAs (sgRNA) as one of the common infection techniques used by these viruses and generally transcribe late viral genes.
Promoter activity is a term that encompasses several meanings around the process of gene expression from regulatory sequences —promoters [2] and enhancers. [3] Gene expression has been commonly characterized as a measure of how much, how fast, when and where this process happens. [ 4 ]
The left model is of the complex of NF-YC/NF-YB with the CCAAT element from the pro- 2(I) collagen promoter. The DNA backbone is shown as ribbons (purple) with the bases displayed. The two possible locations of the CCAAT box, according to the modeling, have been colored cyan. For the right model of the NF-Y/CCAAT complex.
The Pribnow box (also known as the Pribnow-Schaller box) is a sequence of TATAAT of six nucleotides (thymine, adenine, thymine, etc.) that is an essential part of a promoter site on DNA for transcription to occur in bacteria.
The CAG promoter is a strong synthetic promoter frequently used to drive high levels of gene expression in mammalian expression vectors. [1] [2] CAG promoter was constructed in the lab of Dr Jun-ichi Miyazaki [3] [4] from the following sequences: (C) the cytomegalovirus (CMV) early enhancer element,
Promoter bashing is a technique used in molecular biology to identify how certain regions of a DNA strand, commonly promoters, affect the transcription of downstream genes. Under normal circumstances, proteins bind to the promoter and activate or repress transcription.
Further research at the late stage of thymocyte development reveals that distal Lck promoter with driven Cre will result in the distal lck gene promoter to drive Cre expression to be limited within innate-like T cells. There is a cell type specific function in innate-like T cells based on the distal lck promoter - driven Cre. [3]
Thus many chromatin samples can be prepared in parallel and stored, and Q 2 ChIP can be undertaken in a day. [20] MicroChIP (μChIP): chromatin is usually prepared from 1,000 cells and up to 8 ChIPs can be done in parallel without carriers. The assay can also start with 100 cells, but only suit for one ChIP.