Allele specific PCR is used in the process of DNA fingerprinting where specific alleles Can be amplifies and the degree of similarity or difference between individuals can be determined.
A primer (oligonucleotide of a specific sequence) is required for Taq polymerase to extend the template strand by adding complementary nucleotides. The function of the primer is to anneal to the template strand at a very specific site and facilitate the initiation of strand elongation mediated by Taqploymerase.
The laboratory process used to copy specific segments of DNA is called the Polymerase Chain Reaction (or PCR)
The promoter region, typically located upstream of the coding sequence, serves as the recognition site for RNA polymerase. It contains specific DNA sequences that allow RNA polymerase to bind and initiate transcription.
False: its An Repressor not an enhancer
RNA Polymerase
A primer (oligonucleotide of a specific sequence) is required for Taq polymerase to extend the template strand by adding complementary nucleotides. The function of the primer is to anneal to the template strand at a very specific site and facilitate the initiation of strand elongation mediated by Taqploymerase.
PCR stands for "polymerase chain reaction," which is a molecular biology technique used to amplify and detect specific DNA sequences. It is commonly used in medical diagnostics and research to detect viruses, bacteria, and genetic mutations.
The laboratory process used to copy specific segments of DNA is called the Polymerase Chain Reaction (or PCR)
RNA polymerase bind specific regions of DNA called promoters. The RNA polymerase holoenzyme is guided to promoters by interactions between members of the holoenyzme and specific DNA sequences such as the TATA box.
application of archimedes' principle of specific?
There are different types of DNA polymerase depending if it's from a eukaryotic or prokaryotic cell each performing specific tasks. Basically DNA polymerase catalyzes the formation of a polymer, a DNA strand, from many monomers, deoxyribonucleotides.
Miranda Jayne Butler has written: 'Identification of region-specific targets of wingless signalling in Drosophila melanogaster using oligonucleotide microarrays'
The promoter region, typically located upstream of the coding sequence, serves as the recognition site for RNA polymerase. It contains specific DNA sequences that allow RNA polymerase to bind and initiate transcription.
A polymerase is an enzyme that catalyzes the conversion of free nucleotides into a single strand. DNA polymerase differs from RNA polymerase in two major respects: * Like all enzymes, DNA polymerase is substrate-specific. DNA polymerase cannot extend a single strand of DNA; it needs at least a short segment of double-stranded DNA at the outset. * As its name implies, DNA polymerase incorporates deoxyribonucleotides into the new strand. RNA polymerase incorporates ribonucleotides. These differences mean that DNA polymerase is active when new DNA strands are formed, as in DNA replication, and RNA polymerase is active when new RNA is formed, as in transcription. Before DNA replication can begin, the two strands must uncoil, so that each can form a template for free nucleotides to attach to. But DNA polymerase cannot get started with a single strand! In vivo(in the cell) RNA polymerase, which is active in the presence of single-stranded DNA, catalyzes the incorporation of a handful of nucleotides into a new strand. The short length of double-stranded nucleic acid that is produced enables DNA polymerase to swing into action. This still leaves a potential difficulty: the nucleotides incorporated in the presence of RNA polymerase are the wrong sort (ribonucleotides). They are subsequently replaced by DNA polymerase. In vitro (during PCR, the polymerase chain reaction) a primer, specially synthesized in a laboratory, attaches to a specific segment of single-stranded DNA, and the DNA polymerase takes over from there. The primer consists of a short length of single-stranded DNA that uniquely complements a specific DNA segment that is targeted for amplification, for example for forensic analysis.In practice, there are several different DNA polymerases and RNA polymerases in an organism.
False: its An Repressor not an enhancer
The water bath is used in the lab to allow a chemical reaction to occur at a specific temperature. The bath is heated to a precise temperature and the beaker or other container is placed in the bath.
There are different types of DNA polymerase depending if it's from a eukaryotic or prokaryotic cell each performing specific tasks. Basically DNA polymerase catalyzes the formation of a polymer, a DNA strand, from many monomers, deoxyribonucleotides.