I think none of the men are the father, they don’t match the child’s results.
I think I understand your question, but you question has so many errors in it that it doesn't really make sense.
Budding is the predominant mode of asexual reproduction in sponge. Budding is a asexual reproduction in which a new organism develop from outgrowth or from bud due to cell division at one particular site. A small rounded outgrowth on asexually reproducing organism is cabable of developing into new individual
Answer:
boll weevills succes is greatly dependent on its ability to adapt and invade homes this way they are able to live in sheltered areas made by humans and the humans can't get rid of them. a potential way to get rid of them is to find a poison that they'll take for food and that will surely kill them and not just maybe.
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.