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What is the recognition sequence for the BamHI cut site in DNA?
The recognition sequence for the BamHI cut site in DNA is 5'-GGATCC-3'.
Which enzyme would cut the human DNA shown in Part A on both sides of the vgp gene but not inside the gene?
1. Which enzyme(s) would cut the human DNA shown in Part A on both sides of the vgp gene, but not inside the gene? Answer: BamHI, HaeIII, and HindIII 2. Which enzymes(s) would cut the plasmid without disrupting the function of the amp^R gene? Answer: BamHI, EcoRI, and HaeIII 3. Which enzyme(s) would produce sticky ends when cutting both the human DNA and the plasmid? Answer: BamHI, EcoRI, and HindIII 4. Which one restriction enzyme satisfies all three of the requirements listed above? Answer: BamHI only
What are some common design primers with restriction sites used in molecular biology experiments?
Common design primers with restriction sites used in molecular biology experiments include those for enzymes like EcoRI, BamHI, HindIII, and XhoI. These primers are designed to have specific sequences that match the recognition sites of these restriction enzymes, allowing for targeted DNA cleavage and manipulation.
What are the two different restriction enzymes used to cut the pUC19 plasmid and the lux gene DNA?
Two different restriction enzymes commonly used to cut the pUC19 plasmid are EcoRI and PstI. For cutting the lux gene DNA, the restriction enzymes commonly used are NcoI and HindIII.
EcoRI and HindIII are What?
EcoRI and HindIII are restriction enzymes commonly used in molecular biology to cut DNA at specific sequences. They are named after the bacteria species where they were first isolated, Escherichia coli RY13 and Haemophilus influenzae Rd, respectively.
What is the recognition sequence for the BamHI cut site in DNA?
The recognition sequence for the BamHI cut site in DNA is 5'-GGATCC-3'.
How many fragments of DNA would result from BamHI cut sites?
BamHI is a restriction enzyme that recognizes the specific DNA sequence "GGATCC" and cuts between the G and the A. The number of DNA fragments produced by BamHI cutting a DNA molecule depends on the number of BamHI recognition sites present in that molecule. Each recognition site will result in one additional fragment; thus, if there are n cut sites, the DNA will be divided into n+1 fragments.
5 example of palindromic DNA sequences?
Palindromic DNA sequences are segments of DNA that read the same forwards and backwards on complementary strands. Five examples include: 1) EcoRI recognition site: GAATTC, 2) HindIII recognition site: AAGCTT, 3) BamHI recognition site: GGATCC, 4) NotI recognition site: GCGGCCGC, and 5) NheI recognition site: GCTAGC. These sequences are often the target sites for restriction enzymes in molecular biology.
Which enzyme would cut the human DNA shown in Part A on both sides of the vgp gene but not inside the gene?
1. Which enzyme(s) would cut the human DNA shown in Part A on both sides of the vgp gene, but not inside the gene? Answer: BamHI, HaeIII, and HindIII 2. Which enzymes(s) would cut the plasmid without disrupting the function of the amp^R gene? Answer: BamHI, EcoRI, and HaeIII 3. Which enzyme(s) would produce sticky ends when cutting both the human DNA and the plasmid? Answer: BamHI, EcoRI, and HindIII 4. Which one restriction enzyme satisfies all three of the requirements listed above? Answer: BamHI only
What are some common design primers with restriction sites used in molecular biology experiments?
Common design primers with restriction sites used in molecular biology experiments include those for enzymes like EcoRI, BamHI, HindIII, and XhoI. These primers are designed to have specific sequences that match the recognition sites of these restriction enzymes, allowing for targeted DNA cleavage and manipulation.
How many lambda DNA fragments does BamHI make?
There are five BamHI cut sites in lambda DNA: Location 5505 22346 27972 34499 41732 So, BamHI will digest lambda DNA into six fragments.
What is a degradative enzyme that recognizes specific nucleotide sequences and cuts up DNA?
A restriction enzyme is a degradative enzyme that recognizes specific nucleotide sequences and cuts up DNA. These enzymes are often used in biotechnology to cut DNA at specific sites for genetic engineering purposes.
What is the difference between Puc18 and Puc19?
The multiple cloning sites (MCS) in pUC18 and pUC19 is the difference - the MCS in pUC19 is reverse orientated to those of the pUC18.pUC18: LacZ HindIII PaeI ..... SacI EcoRIpUC19: Lacz EcoRI SacI ..... PaeI HindIII
Why use bam h1 ans sau3a1 in plasmid transformation?
BamHI and Sau3A1 are restriction enzymes that can be used to linearize or digest plasmid DNA during the transformation process. Linearizing the plasmid with these enzymes makes it easier for the foreign DNA to be inserted and integrated into the plasmid. This helps in efficiently producing recombinant plasmids with the desired DNA insert.
How restriction enzyms are use in DNA recommination research?
Restriction enzymes are used in DNA recombination research to cut DNA at specific recognition sequences. This allows researchers to generate DNA fragments with desired sequences that can be further manipulated or combined with other DNA fragments to create recombinant DNA molecules. By cutting DNA at precise locations, restriction enzymes facilitate the cloning of genes or the construction of genetically modified organisms.
What are the two different restriction enzymes used to cut the pUC19 plasmid and the lux gene DNA?
Two different restriction enzymes commonly used to cut the pUC19 plasmid are EcoRI and PstI. For cutting the lux gene DNA, the restriction enzymes commonly used are NcoI and HindIII.
EcoRI and HindIII are What?
EcoRI and HindIII are restriction enzymes commonly used in molecular biology to cut DNA at specific sequences. They are named after the bacteria species where they were first isolated, Escherichia coli RY13 and Haemophilus influenzae Rd, respectively.
