1) Do we need to know the differences of transcription and translation in eukaroytes and prokaryotes?
2) What are transcription factors? Do we need to know their function?
3) Do we need to know gene conservation? I've noticed its no longer on the study design anymore
4) To create transgenic organisms, does the inserted DNA have to come from a different species? Or can it just be any foreign DNA
5) Does the genome include ALL genetic material including RNA?
Thanks!
1) I'm fairly certain that we don't need to know about prokaryotic transcription and translation.
2) No. Google image search 'transcription factors' to see what they are if you're curious.
3) It's not in my textbook (N.O.B) or on the study design, so I'm going to assume not.
4) From a different species.
5) Genome is the full set of genes within an individual, so I don't think that includes RNA (unless we're talking about retroviruses, or RNA viruses).
In the allergic response, what actually causes the production of IgE antibodies? these are the steps i have, can somebody please check them??
- organism is exposed to the allergen for the first time
- results in the production of IgE antibodies which travel in the blood stream and bind to mast cell
- mast cells are primed
- second encounter with the allergen produces IgE antibodies which bind to mast cells
- results in the release of histamine, resulting in an allergic respons[/s]e
-organism is exposed to the allergen for the first time
-results in the production of IgE antibodies which travel in the blood stream and bind to mast cell
-Upon re-exposure, the allergenic fragments will cross-link between the IgE antibodies on the mast cells, resulting in the degranulation of the mast cells (histamine released)
-Symptoms of an allergic response thus ensue.
-The immune response increases in significance with each exposure to the allergen, as more antibodies will be produced (by plasma B-cells) against the antigen.
can somebody please explain the process of macrophages and displaying MHC1 markers?
To get it clear, do MHC1 represent non-self? and MHC2 self with damage
-Macrophage encounters a non-self antigen expressed on a pathogen/agent/substance, engulfing it.
-The engulfed substance travels in a vesicle within the macrophage and fuses with a lysosome, where it is broken down into fragments.
-One of these peptide fragments then complexes with an MHC II and is expressed on the plasma membrane of the macrophage.
-Macrophages are APCs, therefore they possess MHC II molecules for the sole purpose of signalling the adaptive immune response upon foreign invasion.
Every nucleated cell (therefore not RBCs) expresses MHC I. Consequently, MHC I are 'self' detectors. As all MHC receptors have the capacity to express peptide fragments, infected cells will have foreign proteins complexed with their MHC I receptors. Normal cells will possess 'self' peptides complexed with their MHC I molecules. This establishes the differentiation between 'self' and 'non-self'
Therefore, MHC I does express 'self', HOWEVER upon infection (say by a virus) the molecules will express obscure peptide fragments which indicates to the immune system that the cell is not healthy. Then, NK cells (antigen non-specific) or Tc cells (antigen specific) will destroy the affected cells.
I hope that makes sense

When describing the existence of variation within a specific population and the effects of natural selection within this population is it more accurate to state that phenotypic variation exists or that genetic variation exists? Any help would be greatly appreciated 
Phenotypic variation, as natural selection works for/against phenotypes rather than discrete genotypes (because hetero/homo dom will express the same phenotype
