A: the F1 generation
Parental cross:: WWDD x wwdd
Possible Gametes for each parent: WD& wd
B: The F2 generation
F1 cross WwDd x WwDd
Possible Gammetes for each parent: WD, Wd,wD, or wd
<span>Tropical Savanna is being converted to a desert biome. When the surface level begins to face advanced erosion, there is less vegetation to hold water in their roots. As the top layer continues to dry out, any new seed being brought in naturally will not be able to grow due to a lack of moisture.</span>
Answer:
Explanation:
In metaphase (a), the microtubules of the spindle (white) have attached and the chromosomes have lined up on the metaphase plate. During anaphase (b), the sister chromatids are pulled apart and move toward opposite poles of the cell.
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.
