Hello there.
<span>Regulation of the cell cycle is dependent upon cyclins and cyclin-dependent kinases. The key(s) that allows a cell to progress beyond the restriction point is (are)
</span><span>c. cyclin A and Cdk2.
</span>
The correct answer is B: The cells will have 2n chromosomes and be diploid.
Diploid cell have two of each chromosome, one from each parent. When diploid cell undergoes mitosis, the result is two identical diploid cells (when haploid cell undergoes mitosis the result is haploid cell). This means that during the mitosis, cells reproduce genetically identical copies of themselves.
Answer:
Gel electrophoresis is a technique used to separate DNA fragments according to their size. DNA samples are loaded into wells indentations at one end of a gel, and an electric current is applied to pull them through the gel. DNA fragments are negatively charged, so they move towards the positive electrode. Really easy
Explanation:
If there isn’t multiple choice I think it is the ones in the center ring (the closest ring to the center) of the atoms
Answer:
1. Map-based genome sequencing: a; c; f; g
2. Whole-genome shotgun sequencing: b
3. Both sequencing methods: d; e
Explanation:
Map-based genome sequencing is a method that makes use of a reference genome sequence in order to determine the relative position of the DNA fragments before they are sequenced. This method is useful to determine the position of repetitive DNA fragments (for example, duplicated genes, repetitive non-coding regions, etc.) and Transposable Elements. Therefore, map-based genome sequencing is a suitable approach for large genomes (which are usually composed of repetitive sequences). On the other hand, in whole-genome shotgun sequencing, DNA sequences are obtained before the correct order of these DNA fragments is known. In this method, the genome is fragmented randomly into small DNA sequences (between 100 and 1000 base pairs), which are subsequently sequenced through the chain-termination sequencing approach (i.e., Sanger sequencing) and finally ordered by using bioinformatic tools that assemble overlapping reads.
