B. Next you isolate DNA from colonies and cut the DNA with the restriction enzymes you chose from question 1. Which lane represents a plasmid that contains the FF1 gene cut with the correct restriction enzyme(s)? 5000bp 1000bp 500bp A B C D E
Molecular Techniques
Molecular techniques are methods employed in molecular biology, genetics, biochemistry, and biophysics to manipulate and analyze nucleic acids (deoxyribonucleic acid (DNA) and ribonucleic acid (RNA)), protein, and lipids. Techniques in molecular biology are employed to investigate the molecular basis for biological activity. These techniques are used to analyze cellular properties, structures, and chemical reactions, with a focus on how certain molecules regulate cellular reactions and growth.
DNA Fingerprinting and Gel Electrophoresis
The genetic makeup of living organisms is shown by a technique known as DNA fingerprinting. The difference is the satellite region of DNA is shown by this process. Alex Jeffreys has invented the process of DNA fingerprinting in 1985. Any biological samples such as blood, hair, saliva, semen can be used for DNA fingerprinting. DNA fingerprinting is also known as DNA profiling or molecular fingerprinting.
Molecular Markers
A known DNA sequence or gene sequence is present on a chromosome, and it is associated with a specific trait or character. It is mainly used as a genetic marker of the molecular marker. The first genetic map was done in a fruit fly, using genes as the first marker. In two categories, molecular markers are classified, classical marker and a DNA marker. A molecular marker is also known as a genetic marker.
DNA Sequencing
The most important feature of DNA (deoxyribonucleic acid) molecules are nucleotide sequences and the identification of genes and their activities. This the reason why scientists have been working to determine the sequences of pieces of DNA covered under the genomic field. The primary objective of the Human Genome Project was to determine the nucleotide sequence of the entire human nuclear genome. DNA sequencing selectively eliminates the introns leading to only exome sequencing that allows proteins coding.
For A. Answer is Culture in ampicillin media to isolate bacteria that took up the plasmid, killing off the bacteria that did not take up the plasmid. Can you explain why?
For B. Answer is Lane C. Can you explain why?
![B. Next you isolate DNA from colonies and cut the DNA with the restriction enzymes you chose from
question 1. Which lane represents a plasmid that contains the FF1 gene cut with the correct restriction
enzyme(s)?
5000bp
1000bp
500bp
A
B
C
D E](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5edaa326-66b2-4fae-a46e-7607d6f7c01e%2Fbb4c8497-3f09-4c9e-9a7e-08e844c44230%2Fa656vz_processed.jpeg&w=3840&q=75)
![Below is a map of the bacterial plasmid and a piece of human genomic DNA that contains the FFI gene.
Xhol
Ori
Plasmid DNA
EcoRII
AmpⓇ
gene
Unique
restriction
sites
BamHI
Alu1
Egli
Xhol
Human genomic DNA
-EcoRII
BamHI
Xhol
-Egli
FFI gene
Xhol
EcoRII
Alu1
The FF1 gene that correctly inserts into the plasmid is 700bp. The plasmid is 5,000bp. You ligate the FF1
gene into the plasmid and transform it into bacteria. How would you know which bacteria successfully took
up the plasmid?
A. How would you know which bacteria successfully took up the plasmid?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5edaa326-66b2-4fae-a46e-7607d6f7c01e%2Fbb4c8497-3f09-4c9e-9a7e-08e844c44230%2Fv37gsnrk_processed.jpeg&w=3840&q=75)
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