State the differences between the plasmid in Figure 1 with pBR322 in terms of their sercening procedures. c)

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c only

Eco01091 20/4
Plai 48
PstAPI 179
Aath 2613
Liet 183
Sspl 2501
Ehel, SspDI 235
Pdmi 2234
Bogl 2215
Scal 2177
Tsol 2108
2456
MCS
BsaX 659
pUC18/19
2686 bp
NmeAlli 1822
Afl, Pscl 806
Gsul 1/84
Ctri0l 17/19,
Eco311 1/66
Eam1105! I691
466
rep (PMB1)
Cail 1217
Psp-i 1110
Figure 1
(https://www.fishersci.com/shop/products/thermo-scientific-puc18-pue19-dna-50-g/fersd0051)
Figure I above is showing the plasmid map of PUC18. Discuss how screening is carried out
if this plasmid is used for cloning.
Explain the THREF. (3) important regions of this plasmid that enable it to work efficiently as
a cloning vector?
b)
State the differences between the plasmid in Figure i with PBR322 in terms of their
sercening procedures.
c)
Discuss TWO (2) methods of transformation of competent bacterial cells with the plasmid in
Figure 1.
d)
bla (Ap)
Transcribed Image Text:Eco01091 20/4 Plai 48 PstAPI 179 Aath 2613 Liet 183 Sspl 2501 Ehel, SspDI 235 Pdmi 2234 Bogl 2215 Scal 2177 Tsol 2108 2456 MCS BsaX 659 pUC18/19 2686 bp NmeAlli 1822 Afl, Pscl 806 Gsul 1/84 Ctri0l 17/19, Eco311 1/66 Eam1105! I691 466 rep (PMB1) Cail 1217 Psp-i 1110 Figure 1 (https://www.fishersci.com/shop/products/thermo-scientific-puc18-pue19-dna-50-g/fersd0051) Figure I above is showing the plasmid map of PUC18. Discuss how screening is carried out if this plasmid is used for cloning. Explain the THREF. (3) important regions of this plasmid that enable it to work efficiently as a cloning vector? b) State the differences between the plasmid in Figure i with PBR322 in terms of their sercening procedures. c) Discuss TWO (2) methods of transformation of competent bacterial cells with the plasmid in Figure 1. d) bla (Ap)
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