Examples of using Nucleotide in English and their translations into Spanish
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Official
Explain the fundamental importance of the phenomenon as"the randomness of being 5'- nucleotide in antikodonah in the homonymous situations in the synthesis of proteins by the Ribosome.
The order in which these nucleotide bases appear in the nucleic acid is the coding for the information carried in the molecule.
In other words, the nucleotide bases serve as a sort of genetic alphabet on which the structure of each protein in our bodies is encoded.
two intracellular nucleotide fixing folds(NFBs: Nucleotide Binding Folds),
The scarcity of nucleotide available for repair
Four different nucleotide bases occur in DNA: adenine(A), cytosine(C),
This protein belongs to a family of proteins called nucleotide binding domain
The nucleotide bases of the DNA molecule form complementary pairs: The nucleotides hydrogen bond to another nucleotide base in a strand of DNA opposite to the original.
Iii Determine the nucleotide sequence of the PCR product
The amplified segments are then compared to other nucleotide segments from a known source to see if that particular DNA segment in the patient sample is present.
the hydrogen bonds between the nucleotide bases break and the two single strands of DNA separate.
These mutations consist of small deletions in exon 19(delL747-A750) or nucleotide substitutions that change the amino acid resulting in exons 18(G719C) and 21 L858R and L861Q.
Also the presence of the nucleotide base has proved to play a significant role in stabilization of the lid in a closed conformation.
Nucleotide sequence of the received copies of the DNA phantom materialized 98% coincides with the origin of donor DNA real data about this prepared for printing.
Like DNA, RNA has a sugar-phosphate backbone with nucleotide bases attached to it.
Though only four different nucleotide bases can occur in a nucleic acid, each nucleic acid
According to the nucleotide variability along its entire sequence differs in 6 genotypes when the differences are 30 to 35% of its nucleotide sequence.
Mutations in patients with these latter forms are due to nucleotide substitutions that affect mRNA.
Mutations that result registered variants mentioned above are nucleotide, insertions, deletions and alterations of copy number.
to a third type of molecule called a nucleotide base.