TLS Online TPP Program
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TLS Online TPP Program
#Question id: 3681
#SCPH06 I Botany
A mutated E. coli cell carries out and completes DNA replication, but the lagging strands are found to contain more errors than normal. These errors are not found evenly distributed throughout the lagging strands, but are found in clusters. Which enzymatic activity is missing from this cell?
TLS Online TPP Program
#Question id: 5214
#SCPH28 | Zoology
What is the most probable explanation for the continued presence of pseudogenes in a genome such as our own?
TLS Online TPP Program
#Question id: 19598
#SCPH05 I Biotechnology
Considering entropy(S) thermodynamic parameters the criteria for the spontaneity of any process is:
TLS Online TPP Program
#Question id: 12749
#SCPH28 | Zoology
What are the constituents used for isolation of bacterial plasmid DNA, RNA and plant DNA respectively?
TLS Online TPP Program
#Question id: 13088
#SCPH05 I Biotechnology
To express a yeast gene in E. coli, your task is to design a strategy to insert the yeast gene into the bacterial plasmid. Below is a map of the area of the yeast genome surrounding the gene in which you are interested.
The distance between each tick mark placed on the line above is 100 bases in length
Below are the enzymes you can use, with their specific cut sites shown 5’-XXXXXX-3’ 3’-XXXXXX-5’
The plasmid is 5,000 bases long and the two farthest restriction enzyme sites are 200 bases apart. The plasmid has an ampicillin resistance gene somewhere on the plasmid distal from the restriction cut sites.
You do the digestion of the insert and the vector and then ligate the two digestions together. You then transform the ligation into bacteria and select for ampicillin resistance. You get three colonies on your transformation plate. You isolate plasmid from each one and cut each plasmid with the enzyme XbaI. You then run your three digestions on an agarose gel and see the following patterns of bands. Describe what each plasmid actually was that was contained in each of the three colonies.
What is the Colony 1’s plasmid is;