The researchers further investigated the untransformed porcine fibroblasts as well as the AB1 neomycin resistant clone in a PCR-RFLP (restriction fragment length polymorphism) experiment. Genomic DNA from the untransformed porcine fibroblasts as well as the AB1 neomycin resistant clone was used in a PCR reaction using the primer pair H/B as illustrated below. Following PCR the products were subject to restriction enzyme digestion with Smal (sites indicated in the figure below). Sal-ike 1 locus F E1 Targeted locus H E2 1660 bp PCR primer H 167bp PCR primer H -Smal Smal 2854 2684 bp PGK-neo bp ←Smal E3 PCR primer B POR primer B 1834 bp

Human Anatomy & Physiology (11th Edition)
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Chapter1: The Human Body: An Orientation
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) Clearly and neatly diagram an image of the agarose gel indicating the fragments that would be generated from PCR of genomic DNA templates derived from an untransformed porcine cell line, a cell line in which there had been a monoallelic targeting event, and a cell line in which there had been a biallelic targeting event when using the primer pair H/B, if the PCR product(s) were digested with SmaI prior to electrophoresis. Illustrate the fragments and their sizes that would have been visualized on the gel. Note - now there has been digestion of the PCR product(s) with SmaI prior to electrophoresis
The researchers further investigated the untransformed porcine fibroblasts as well as the AB1 neomycin
resistant clone in a PCR-RFLP (restriction fragment length polymorphism) experiment. Genomic DNA from the
untransformed porcine fibroblasts as well as the AB1 neomycin resistant clone was used in a PCR reaction
using the primer pair H/B as illustrated below. Following PCR the products were subject to restriction enzyme
digestion with Smal (sites indicated in the figure below).
Sal-like 1 locus
H
E1
Targeted locus
H
E2,
1660
PCR primer H
PCR primer H
167bp
bp
-Smal
Smal
2854
2684 bp
PGK-neo
bp
←Smal
E3
PCR primer B
POR primer B
1834 bp
Transcribed Image Text:The researchers further investigated the untransformed porcine fibroblasts as well as the AB1 neomycin resistant clone in a PCR-RFLP (restriction fragment length polymorphism) experiment. Genomic DNA from the untransformed porcine fibroblasts as well as the AB1 neomycin resistant clone was used in a PCR reaction using the primer pair H/B as illustrated below. Following PCR the products were subject to restriction enzyme digestion with Smal (sites indicated in the figure below). Sal-like 1 locus H E1 Targeted locus H E2, 1660 PCR primer H PCR primer H 167bp bp -Smal Smal 2854 2684 bp PGK-neo bp ←Smal E3 PCR primer B POR primer B 1834 bp
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