To determine the base sequence of DNA fragments on both sides of a cut, you would need to know the specific location and context of the cut made by a restriction enzyme or other DNA manipulation technique. Generally, the left side fragment will represent the sequence leading up to the cut site, while the right side fragment will contain the sequence that follows it. Without the specific sequence or context, it is impossible to provide the exact base sequences.
The restriction enzyme used cuts the DNA at specific recognition sites, resulting in fragments of various sizes based on the distribution of these sites along the DNA molecule. In this case, the enzyme produced DNA fragments of 4000, 2500, 2000, and 400 base pairs in length after digestion. These specific sizes are a result of the locations of the recognition sites for that particular restriction enzyme along the DNA sequence.
The base sequence of mRnas is 'determined by the base sequence of nucleotides in Dna.' The base sequence is transformed into information via the triplet codons of The Genetic Code.
ATAGCC is complementary to the base sequence TATCGG.
You can predict the base sequence of one strand of DNA if you know the sequence of the other strand because DNA strands are complementary. Adenine (A) pairs with thymine (T), and cytosine (C) pairs with guanine (G). This complementary base pairing allows the sequence of one strand to dictate the sequence of the other, enabling accurate predictions of the base sequence.
To determine the base sequence of DNA fragments on both sides of a cut, you would need to know the specific location and context of the cut made by a restriction enzyme or other DNA manipulation technique. Generally, the left side fragment will represent the sequence leading up to the cut site, while the right side fragment will contain the sequence that follows it. Without the specific sequence or context, it is impossible to provide the exact base sequences.
TACA
Okazaki fragments are typically around 100-200 base pairs long in prokaryotes and around 1000-2000 base pairs long in eukaryotes.
The restriction enzyme used cuts the DNA at specific recognition sites, resulting in fragments of various sizes based on the distribution of these sites along the DNA molecule. In this case, the enzyme produced DNA fragments of 4000, 2500, 2000, and 400 base pairs in length after digestion. These specific sizes are a result of the locations of the recognition sites for that particular restriction enzyme along the DNA sequence.
The base sequence of mRnas is 'determined by the base sequence of nucleotides in Dna.' The base sequence is transformed into information via the triplet codons of The Genetic Code.
ATAGCC is complementary to the base sequence TATCGG.
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You can predict the base sequence of one strand of DNA if you know the sequence of the other strand because DNA strands are complementary. Adenine (A) pairs with thymine (T), and cytosine (C) pairs with guanine (G). This complementary base pairing allows the sequence of one strand to dictate the sequence of the other, enabling accurate predictions of the base sequence.
The mRNA base sequence corresponding to the DNA sequence acgtt is ugcaa. The mRNA sequence is complementary to the DNA sequence, with thymine (T) in DNA being replaced by uracil (U) in mRNA.
TACA
The sequence shown is "ACAGTGC".
what is a practical or clinical use of knowing the base sequence of a gene