Answer: a. tRNA
Explanation: The transference RNA is a nucleic acid that participates of the protein synthesis. tRNA is a small RNA with folding as a trefoil. The tRNA has a site where aminoacid is loaded and a anticodon site that is complementary to the codon in the mRNA, ensuring the proper aminoacid sequence in the resulting polypeptide.
Adenosine triphosphates glycogen I believe
<span>The fluid flows through the interventricular foramen into the third ventricle, is augmented by fluid formed by the choroid plexus of this ventricle, and passes through the cerebral aqueduct to the fourth ventricle, which also possesses a choroid plexus. The CSF from all theses sources , as well as any formed in the central canal of the spinal cord, escapes from the fourth ventricle into the subarachnoid space through the median aperture and lateral aperture.</span>
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.
