That's simple.
To see which enhancer is active at what site, we just need to put the beta galactosidase gene with the individual promoters, in different plasmids. For example, here we need four types of constructs, each having one enhancer sequence (and obviously, the promoter sequence) upstream to the beta-galactosidase coding gene. If the enhancer is active, it will cause beta-galactosidase to express, which will produce blue colour in presence of X-gal.
When we do not know the functions of enhancers, we need to express such kinds of constructs in different embryos and see which sites produce blue colour, to know which sites the enhancer is active in. Since only the lens/cornea and pancreas get blue colour, the construct should be like this -
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Assignment 1. - Word File Insert Design Layout References Mailings Review View Tell me what you...
Assignment 1. - Word File Insert Design Layout References Mailings Review View Tell me what you want to do Sign in Share Home Cut Find Aria E Copy Paste Select Editing Format Painter Clipboard Paragraph Font 9 leads to cell division when the target gene is transcribed. When the signal is present, will the target gene be Styles (5) The following is a diagram of the RTK signalling pathway. Assume that when the signal is present the pathway Ligand Receptor...