The phylum Echinodermata , which contains about 6000 species, gets its name from the Greek, literally meaning "spiny skin." Many echinoderms actually do have "spiny" skin, but others do not. This phylum exists exclusively in the sea, and cannot be found on land or in fresh water. All echinoderms have one thing in common: radial symmetry. This means that the creatures have appendages (or body construction) which point outward from the center of the body like the spokes on a bicycle wheel. Furthermore, these appendages usually occur in multiples of five, although there are a few exceptions. There are several well known members of this group, like sea stars and sea urchins. The radial symmetry is obvious in these creatures.
Answer:
Hydrogen Bonds
Explanation:
In the polymerase chain reaction (PCR) the temperature rises to 90 ° C - 95 ° C, to break the hydrogen bonds, which are the types of bonds responsible for pairing the two strands of DNA, this process is known as denaturation of DNA.
The DNA is extremely stable, due to a large number of bonds (hydrogen bonds) that form between the two strands. If the temperature decreases, these bonds will begin to recompose, until the DNA returns to its original state
Answer:
Cell division or cytokinesis in mitosis or meiosis is very similar... There is a region of division to separate the two daughter cells in both processes; however, the division plate is slightly different between animal cells and plant cells. In animals, the region of division is a division plate. hope this helps! :)
The main idea is that microorganisms are small and they live everywhere possible.
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.
