Well DNA can't really be in a simple explanation. It is a deoxyribonucleic acid that strands our genetic material together into a double-stranded genome. Not that simple really. All the theories and definitions complicate it way past what it should be. DNA is made up of genes which are made up of chromosomes and nucleotides. Every person with no mutation have 46 total or 23 pairs of chromosomes, 23 from their birth mother and 23 from their birth father. If there is more than 46 total it is classified as a mutation, although nothing maybe wrong with t individual person, and there could always be a physical defect from that. Nucleotides are what the double-stranded helix of DNA is made from. Pairs of molecules; the only four of which are involved are: Adenine (A), Thymine (T), Guanine (G), and Cytosine (C). They pair up as A to T and C to G. Unless it is RNA, those will always pair as that. In RNA the Adenine isn't there, is 'traded' for Uracil (U). So yeah - not all that simple. :)
The short strand of DNA is called the primer. It serves as a starting point for DNA replication by providing a free 3' end for DNA polymerase to begin synthesis. Primers are typically about 18-22 nucleotides long and are complementary to the template DNA strand.
A short tandem repeat or STR is a type of polymorphism, where short sequences of DNA are repeated. It is a useful tool in forensics because the number of times a DNA sequence is repeated for a given STR varies between individuals.
Short tandem repeat DNA is useful for DNA fingerprinting because it contains repeating sequences of 2-6 base pairs that can vary in length between individuals. This variation creates unique DNA profiles that can be used to differentiate between individuals. The high variability and stability of STRs make them ideal for forensic analysis and paternity testing.
Short strands of DNA move more quickly than long strands because they are smaller and can navigate through obstacles more easily.
DNA polymerase III requires a primer, which is a short piece of RNA or DNA, in order to function correctly.
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Polymerase chain reaction (PCR) is a common method used to assemble short sequences of DNA. PCR requires a DNA template, primers (short DNA sequences that flank the target region), DNA polymerase enzyme, nucleotides, and a thermal cycler to amplify the DNA target region through repeated cycles of denaturation, annealing, and extension.
The short strand of DNA is called the primer. It serves as a starting point for DNA replication by providing a free 3' end for DNA polymerase to begin synthesis. Primers are typically about 18-22 nucleotides long and are complementary to the template DNA strand.