The data are not found here, but evolution means 'descendence with modification', which may occur due to natural selection and mutations.
<h3>What is evolution?</h3>
Evolution is descendence with modification, which generally is caused by a process called natural selection.
Natural selection 'selects' the most adaptive variants in the population, which occurs due to the emergence of mutations.
A mutation is any genetic change in the nucleotide sequence of the genome of an individual.
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Answer:
Cations are ions that are positively charged. They form when they lose an electron because they would have more protons than electrons. In your problem you have for example potassium (number three).
Iodine is a cation because it lost one electron. The ion symbol then would be:
I ⁺
So this is your clue. If it has a positive or a plus sign on top, that would make it a cation. Another clue would be if it LOST an electron, then it is a cation.
An anion, on the other hand, is negatively charged, because they gain electrons, making the electrons more than the protons. In your problem, you have Iodine as an example (number one).
Iodine gained one electron and the ion symbol would be:
I⁻
So again that is your clue for anions, they have a negative or a minus sign on top of the symbol. If they GAINED an electron, that would make them an anion.
Naming monoatomic anions is easy. They are named with the suffix -ide at the end. (Cations retain their name). For example Sulfur (number two).
Sulfur is an anion that gained two electrons with an ion symbol of:
S²⁻
So from the name <u>Sulfur</u><u> </u>the name will change into "Sulfide" and its name will now be <u>Sulfide ion. </u>
The messenger RNA is a single-stranded intermediate
molecule that transfers the genetic information from DNA to the cytoplasm,
which is used as a template to assemble the chain of amino acids that form a variety of polypeptides. Therefore, mRNA is the blueprint for
protein synthesis, which is read according to the genetic code during gene
expression.
Answer:
Background
During the course of a bacterial infection, the rapid identification of the causative agent(s) is necessary for the determination of effective treatment options. We have developed a method based on a modified broad-range PCR and an oligonucleotide microarray for the simultaneous detection and identification of 12 bacterial pathogens at the species level. The broad-range PCR primer mixture was designed using conserved regions of the bacterial topoisomerase genes gyrB and parE. The primer design allowed the use of a novel DNA amplification method, which produced labeled, single-stranded DNA suitable for microarray hybridization. The probes on the microarray were designed from the alignments of species- or genus-specific variable regions of the gyrB and parE genes flanked by the primers. We included mecA-specific primers and probes in the same assay to indicate the presence of methicillin resistance in the bacterial species. The feasibility of this assay in routine diagnostic testing was evaluated using 146 blood culture positive and 40 blood culture negative samples.
Explanation:
Results
Comparison of our results with those of a conventional culture-based method revealed a sensitivity of 96% (initial sensitivity of 82%) and specificity of 98%. Furthermore, only one cross-reaction was observed upon investigating 102 culture isolates from 70 untargeted bacteria. The total assay time was only three hours, including the time required for the DNA extraction, PCR and microarray steps in sequence.