1. You make a recombinant plasmid vector that contains an insert of a gene you are interested in studying (see below on left). After making your recombinant vector you run it on an agarose gel to check it (See below on right). You run some of the uncut vector and see 3 bands (Uncut lane). You also cut some recombinant vector with both restriction enzymes BamHI and HindIII and run this on the gel too (Cut lane). Agarose Gel Recombinant Plasmid vector with insert -ve BamHI insert Hindi- bp 5,000 2,300 2,000 1,800 1,000 500 300 DNA Marker Uncut A B Cut D +ve

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 Q. What is the total size of your recombinant plasmid vector containing the insert?  

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1. You make a recombinant plasmid vector that contains an insert of a gene you are interested in studying
(see below on left). After making your recombinant vector you run it on an agarose gel to check it (See
below on right). You run some of the uncut vector and see 3 bands (Uncut lane). You also cut some
recombinant vector with both restriction enzymes BamHI and HindIII and run this on the gel too (Cut
lane).
Agarose Gel
Recombinant Plasmid vector
with insert
-ve
BamHI
insert
Hind 11-
bp
5,000
2,300
2,000
1,800
1,000
500
300
DNA
Marker Uncut
B
Cut
+ve
Transcribed Image Text:1. You make a recombinant plasmid vector that contains an insert of a gene you are interested in studying (see below on left). After making your recombinant vector you run it on an agarose gel to check it (See below on right). You run some of the uncut vector and see 3 bands (Uncut lane). You also cut some recombinant vector with both restriction enzymes BamHI and HindIII and run this on the gel too (Cut lane). Agarose Gel Recombinant Plasmid vector with insert -ve BamHI insert Hind 11- bp 5,000 2,300 2,000 1,800 1,000 500 300 DNA Marker Uncut B Cut +ve
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