Hae III cuts at the site GGCC. It creates blunt ends - meaning a clean cut. This is found between the G and C.
The restriction site of Hae III is GGCC. It cuts between the G and the C. This produces blunt ends.
Restriction enzymes are endonucleases that digest the DNA at a sequence specific site. Hind III for example cut between two As in the sequence AAGCTT in the both strand forming a sticky end. If you use this enzyme to cut in your vector DNA, you have to use the same enzyme in the insert DNA so as they can ligate by DNA ligation. This is the important use of same restriction enzyme in cloning.
DNA Polymerase is the enzyme which adds new nucleotides during replication.
THat would be the enzyme DNA Polymerase III which attaches free floating nucleotides to the parent strand. But remember, they can only be attached to a free 3' position!
DNA polymerase III
The restriction site of Hae III is GGCC. It cuts between the G and the C. This produces blunt ends.
She was able to do so because the band pattern portrayed on the agarose gel shows exactly where the sequence AAGCTT was located on the DNA. Because of this, she was able to place the Hind III restriction enzyme right at that sequence since it was given that the enzyme recognizes that specific sequence.
Restriction enzymes are endonucleases that digest the DNA at a sequence specific site. Hind III for example cut between two As in the sequence AAGCTT in the both strand forming a sticky end. If you use this enzyme to cut in your vector DNA, you have to use the same enzyme in the insert DNA so as they can ligate by DNA ligation. This is the important use of same restriction enzyme in cloning.
Restriction enzymes are named based on the organism in which they were discovered. For example, the enzyme Hind III was isolated from Haemophilus influenzae, strain Rd. The first three letters of the name are italicized because they abbreviate the genus and species names of the organism. The fourth letter typically comes from the bacterial strain designation. The Roman numerals are used to identify specific enzymes from bacteria that contain multiple restriction enzymes. Typically, the Roman numeral indicates the order in which restriction enzymes were discovered in a particular strain.There are three classes of restriction enzymes, labeled types I, II, and III. Type I restriction systems consist of a single enzyme that performs both modification (methylation) and restriction activities. These enzymes recognize specific DNA sequences, but cleave the DNA strand randomly, at least 1,000 base pairs(bp) away from the recognition site. Type III restriction systems have separateenzymes for restriction and methylation, but these enzymes share a common subunit. These enzymes recognize specific DNA sequences, but cleave DNA at random sequences approximately twenty-five bp from the recognition sequence. Neither type I nor type III restriction systems have found much application in recombinant DNA techniques.Type II restriction enzymes, in contrast, are heavily used in recombinant DNA techniques. Type II enzymes consist of single, separate proteins for restriction and modification. One enzyme recognizes and cuts DNA, the other enzyme recognizes and methylates the DNA. Type II restriction enzymes cleave the DNA sequence at the same site at which they recognize it. The only exception are type IIs (shifted) restriction enzymes, which cleaveDNA on one side of the recognition sequence, within twenty nucleotides of the recognition site. Type II restriction enzymesdiscovered to date collectively recognize over 200 different DNA sequences.
DNA Polymerase III
RNA polymerase
I, II, and III I. It is the rate-limiting enzyme of glycogenolysis II. It breaks alpha 1,4 glycosidic bonds III. It is activated by epinephrine
the DNA polymerase III
HinD III and Bam HI
The enzyme that transcribes the DNA into RNA is called RNA polymerase.
DNA polymerase III .
DNA Polymerase is the enzyme which adds new nucleotides during replication.