TLS Online TPP Program

#Question id: 3870


“Footprinting” or DNase protection is a technique used to identify:

#Section 3: Genetics, Cellular and Molecular Biology
  1. a region of DNA that has been damaged by mutation.

  2. E. coli cells that contain a desired, cloned piece of DNA.

  3. the position of a particular gene of a chromosome.

  4. the specific binding site of a repressor, polymerase, or other protein on the DNA.

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TLS Online TPP Program

#Question id: 16846

#General Aptitude

Head Over Heels

TLS Online TPP Program

#Question id: 13093

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

You are studying a specific gene in yeast, and you want to express that 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 transform your ligation planned in which two restriction enzymes would you use to design a way to get the insert into the vector if you had to use two enzymes simultaneously, into bacteria and plate the bacteria on Petri plates containing ampicillin. (You actually transform six different ligation mixtures, which are described below, into six different populations of cells, and plate each transformation onto a different plate, because you want to do all of the correct controls.) The next day you come in to lab to look at how many colonies of bacteria are on each plate. You are really excited, because the number of colonies you see on each plate tells you that the entire procedure worked! Which of the three following patterns of number of colonies did you see in order to conclude that you had a successful transformation?
In this table, DV = digested vector. DYG = digested yeast genome.
 

TLS Online TPP Program

#Question id: 12936

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Adding small double-stranded molecules with one internal site for a restriction endonuclease,termed ______ to cDNA.

TLS Online TPP Program

#Question id: 14090

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Which of the following is an example of a primary protein sequence database?

TLS Online TPP Program

#Question id: 2119

#Section 3: Genetics, Cellular and Molecular Biology

A sodium-potassium pump: