GCTAATCA because A pairs with T and C pairs with G always, so you just have to match them up! Took me a while to figure it out, too...(:
The DNA sequence that would pair with the DNA segment TTACGC is AATGCG. The mRNA sequence that would pair with the DNA segment TTACGC is AAUGCG.
Single nucleotide polymorphisms (SNPs) are commonly used to distinguish one sequence of DNA from another by comparing sequence strands at specific loci. SNPs are variations at a single base pair in DNA, making them useful for identifying differences between individuals or populations.
Yes, when a DNA base pair is mismatched during duplication, it can lead to a mutation in the DNA sequence. This can cause changes in the protein produced, potentially impacting the function of the gene and, ultimately, the organism.
In DNA, the sequence of bases that would pair with GTACG would be CATGC. In RNA, the sequence of bases that would pair with GTACG would be CAUGC, because in RNA, uracil (U) replaces thymine (T).
The nucleotide sequence in DNA is determined by the sequence of the nitrogenous bases (adenine, thymine, cytosine, and guanine) along the DNA strand. These bases pair up in specific ways: adenine with thymine and cytosine with guanine. The order in which these bases are arranged along the DNA molecule determines the genetic information encoded within the DNA.
The DNA sequence that would pair with the DNA segment TTACGC is AATGCG. The mRNA sequence that would pair with the DNA segment TTACGC is AAUGCG.
No. DNA is not put together randomly. The sequence of DNA is specific to the genes that control the cell's activities and heredity. Each gene has its unique sequence.
The 2nd strand matching DNA refers to the strand that can pair with the original DNA sequence through complementary base pairing. In DNA replication, this matching strand is synthesized by DNA polymerase according to the sequence on the original template strand.
The complementary RNA sequence that would pair with the DNA sequence TACTGCA is AUGACGU. This is because in RNA, uracil (U) is used instead of thymine (T) to pair with adenine (A), cytosine (C) pairs with guanine (G), and vice versa.
It's complimentary pair. C--G and T--A
The base sequence for the complementary DNA would be GCA AT. Since DNA strands are complementary, the bases pair as follows: A with T, T with A, C with G, and G with C.
Single nucleotide polymorphisms (SNPs) are commonly used to distinguish one sequence of DNA from another by comparing sequence strands at specific loci. SNPs are variations at a single base pair in DNA, making them useful for identifying differences between individuals or populations.
Yes, when a DNA base pair is mismatched during duplication, it can lead to a mutation in the DNA sequence. This can cause changes in the protein produced, potentially impacting the function of the gene and, ultimately, the organism.
The DNA segment ttacgc would pair with the complementary RNA sequence aaugcg during replication. In RNA, adenine (A) pairs with uracil (U) instead of thymine (T).
In DNA, the sequence of bases that would pair with GTACG would be CATGC. In RNA, the sequence of bases that would pair with GTACG would be CAUGC, because in RNA, uracil (U) replaces thymine (T).
It is important for cell to copy DNA without making mistake because the DNA contain genetic code in the form of nucleotide base pair sequence, if those sequence get wrong then the DNA code for wrong gene i.e. there will be a mutation which can be lethal or dangerous.
The nucleotide sequence in DNA is determined by the sequence of the nitrogenous bases (adenine, thymine, cytosine, and guanine) along the DNA strand. These bases pair up in specific ways: adenine with thymine and cytosine with guanine. The order in which these bases are arranged along the DNA molecule determines the genetic information encoded within the DNA.