TLS Online TPP Program

#Question id: 12924


In order to quantify unknown DNA templates, a standard dilution is prepared using DNA of known concentration. As the DNA accumulates during the early exponential phase of the reaction,an arbitrary point is taken where each of the diluted DNA samples cross. This is termed as_____

#SCPH01 Biochemistry
  1. Ct Value
  2. Pt value
  3. At Value
  4. St value
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TLS Online TPP Program

#Question id: 5229

#SCPH28 | Zoology

Two eukaryotic proteins have one domain in common but are otherwise very different. Which of the following processes is most likely to have contributed to this phenomenon?

TLS Online TPP Program

#Question id: 13026

#SCPH06 I Botany

A blunt ended insert can not be ligated with a blunt ended vector by means of which of the followings:-

TLS Online TPP Program

#Question id: 2263

#SCPH05 I Biotechnology

Proteins synthesized by the rough ER are

TLS Online TPP Program

#Question id: 2329

#SCPH28 | Zoology

Which of the following would be a problem for a cell if it were able to grow to twice its normal size?

TLS Online TPP Program

#Question id: 13089

#SCPH28 | Zoology

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 2’s plasmid is;