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The genetic code is based on a 3 base sequence because the anticodon on the transfer RNA consists of a 3 base sequence. Each transfer RNA carries one amino acid, and the anticodon, the area that attaches to the corresponding codon in the messenger RNA during translation, is only 3 bases long.

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What is difference between DNA probe and primer?

A DNA probe is a single-stranded DNA sequence used to detect complementary sequences, whereas a primer is a short single-stranded DNA sequence used to initiate DNA synthesis during PCR. Probes are used to identify specific sequences in a sample, while primers are used to amplify a specific target sequence.


What are genes divided into?

The Divisions of the Gene are these: the Up - upstream enhancer sequences, the Upstream promoter sequences, the Operator Sequence that positions the Gene Polymerase Enzyme at the Start Codon, the Coding Sequence, and the Termination 'arrangement' [there are several Forms].


What are small single strands of DNA that will bind with a specific sequence?

Small single strands of DNA that bind to specific sequences are known as oligonucleotides. These synthetic DNA fragments typically range from 15 to 30 nucleotides in length and are designed to hybridize with complementary DNA or RNA sequences. Oligonucleotides are widely used in various applications, including PCR, DNA sequencing, and gene editing. Their specificity allows them to target particular genetic sequences for research and therapeutic purposes.


Where is the information in DNA and rna carried?

The information in DNA is carried in its sequence of nucleotides, which form genes that encode for proteins and regulate cellular functions. In RNA, the information is carried in a single-stranded molecule that is transcribed from DNA and includes messages for protein synthesis.


Are no two nucleotide sequences in DNA molecules ever the same?

Yes. This can happen via a gene duplication in a single organism or by shear coincidence (though its increasingly unlikely the biggest the sequence in question). Identical sequences can happen across species due to heredity from a common ancestor of a common gene or genetic marker, such as we see in ERVs and analysis from computational genomics.

Related Questions

How to combine two sequences in Premiere Pro?

To combine two sequences in Premiere Pro, you can simply drag one sequence into another sequence in the timeline. This will merge the two sequences together, allowing you to create a single, combined sequence.


What two different sequences that are multiples of number sequence 1 4 7?

147 is a single number, it is not a sequence.


How is a SNP identified in an alignment?

A SNP (Single Nucleotide Polymorphism) is identified in an alignment by comparing the DNA sequences of different individuals or species. A SNP is a variation at a single nucleotide position in the DNA sequence. By aligning the sequences and looking for differences at specific positions, researchers can identify SNPs.


How do you get the sequence of 3354435543?

3354435543 is a single number, it is not a sequence.3354435543 is a single number, it is not a sequence.3354435543 is a single number, it is not a sequence.3354435543 is a single number, it is not a sequence.


What is the important of the cells ability to copy single DNA sequence into RNA?

The ability to copy a single DNA sequence into RNA makes it possible for a single gene to produce hundreds or even thousands of RNA molecules.


What is difference between DNA probe and primer?

A DNA probe is a single-stranded DNA sequence used to detect complementary sequences, whereas a primer is a short single-stranded DNA sequence used to initiate DNA synthesis during PCR. Probes are used to identify specific sequences in a sample, while primers are used to amplify a specific target sequence.


What is a complete list of nucleotide sequence in a individuals chromosome?

It is not possible to provide a complete list of nucleotide sequences on an individual's chromosome in a single answer, as each chromosome contains millions of nucleotides. The human genome has over 3 billion base pairs, which make up the DNA on 23 pairs of chromosomes. The sequence can vary between individuals due to genetic variations.


What are genes divided into?

The Divisions of the Gene are these: the Up - upstream enhancer sequences, the Upstream promoter sequences, the Operator Sequence that positions the Gene Polymerase Enzyme at the Start Codon, the Coding Sequence, and the Termination 'arrangement' [there are several Forms].


What are small single strands of DNA that will bind with a specific sequence?

Small single strands of DNA that bind to specific sequences are known as oligonucleotides. These synthetic DNA fragments typically range from 15 to 30 nucleotides in length and are designed to hybridize with complementary DNA or RNA sequences. Oligonucleotides are widely used in various applications, including PCR, DNA sequencing, and gene editing. Their specificity allows them to target particular genetic sequences for research and therapeutic purposes.


What is the sequence for 100?

There is no sequence for a single number.


Where is the information in DNA and rna carried?

The information in DNA is carried in its sequence of nucleotides, which form genes that encode for proteins and regulate cellular functions. In RNA, the information is carried in a single-stranded molecule that is transcribed from DNA and includes messages for protein synthesis.


What number is missing in the squence 17298?

17298 is a single number, not a sequence - or squence even.17298 is a single number, not a sequence - or squence even.17298 is a single number, not a sequence - or squence even.17298 is a single number, not a sequence - or squence even.