Schizocoely is a process by which some animal embryos develop while splitting the mesodermal embryonic tissue. On the other hand, <span> enterocoelous was formed </span><span>in which the coelom forms from pouches "pinched" off of the digestive tract.</span>
If this division is based on tissue formation then it is correct because there are 8 types of cells. If it's based on the function then it's incorrect because there are more than 10.
Answer:
large central vacuole
Explanation:
mature plant cell contains large vacuoles while a animal cell has small vacuoles
Answer:
38 ATP
Explanation:
On complete oxidation of one molecule of glucose yields 38 ATP. Break up of energy production is given below:
- During glycolysis 2 ATP and 2 NADH is produced.
- During formation of Acetyl CoA, 2 NADH is produced.
- During Citric Acid Cycle, 2 ATP, 6 NADH, 2 FADH₂ are produced.
Finally during Electron transport chain, reduced coenzymes NADH and FADH₂ oxidised to release ATP. Each NADH produce 3ATP and each FADH₂ produces 2 ATP. Altogether 10 NADH is produced during entire process of cellular respiration which yield 30 ATP and 2 FADH₂ yields 4 ATP. Therefore, on complete oxidation of one molecule of glucose yields 38 ATP.
Answer:
I think the question is "How might an RNA-based genome results display an increased in infection rate?" because current statement doesn't convey a message clearly.
Explanation:
To answer this question, we need to understand first that what is gene expression. Gene expression is a process in which genetic information is transcribed first to RNA and then into proteins. During transcription stage, only active genes would be transcribed to RNA and all other DNA material don't transcribe at all. Now, if there is an infection, host cell would express only those genes which would actively take part in the defense mechanism, e.g. R-genes, genes involved in production of reactive oxygen species, etc. Hence, to monitor the infection rate, we will look at the RNA-based genome. To do this, we will extract the total RNA and then would sequence it. Then we will annotate the genes and check the relative abundance (differential expression). Finally, we would have a clear that these genes were active against the infection. By doing temporal sampling and sequencing, we would be able to measure the rate as well.
For the second part, potential complications that could arise in doing analysis is the lower amount of RNA, or rapid degradation of RNA in case of presence of RNAses. RNA can be degraded easily at room temperature.
