To see a list of all the enzymes being displayed, the number of times they cut,ĮcoRI folder to see the position of the two EcoRI sites. Open the Restriction/Methylation Map folder in the text pane Click OK to get pNIG6 to be displayed the way we want to see all our This profile does not include any motifs (short DNA or Protein Options, for example, how the sequence is viewed, what restriction sites willīe shown, what motifs are shown, and so on. Pull down the setup profile window and choose The content of pull down menus can alsoĬhange depending on which pane is active.Ĭlick on the display setup icon next to the seq pane. This reflects the fact that differentįunction can be performed depending on which pane is active. Graphics panes change as you move from text to graphics to sequence. Move between panes by clicking in the pane or on the pane icons. The pNIG6 window has three panes: the text pane, the Look at the plasmid that will be the focus of the first three experiments, Window on the right lists ALL DNA/RNA molecules loaded in this database, which Notice that there are databases for proteins, enzymes, oligonucleotides, gel Markers, The window on the left lists the types of databases and the subsets in The database by clicking the toolbar icon. The results of our manipulations of those DNA molecules. Visualize the DNA molecules we will be working with and to predict and analyze We will be using Vector NTI thoughout the second half of BIO 510 to You to Vector NTI software, which is common application for storing, manipulating,Īnd analyzing DNA/RNA/PROTEIN sequences.
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