The λ PE promoter is known to have a weak promoter. Explain the reason for this by comparing the λ PE promoter -35 element to a consensus -35 element.
Every gene contains a promoter region before the presence of the start sequence for transcription. The RNA polymerase binds to the gene by identifying the molecular sequence of the promoter region. The nature of interaction between the RNA polymerase and the promoter region has been evolved in a manner such that presence of a consensus and conserved sequence determines the extent of binding of RNA polymerase to the promoter. Any deviation from the consensus and conserved sequence of this upstream promoter region, i.e. the -35bp pCG sequence and the -10bp TATA box, lead to either loose binding of the RNA polymerase or altogether failure of binding.
Even under cases of loose binding of RNA polymerase, the gene expression is significantly down-regulated. This is because the loose binding leads to frequent disconnection between the gene sequence and the RNA polymerase thus preventing constant and un-interrupted movement of the RNA polymerase on the gene. This is why genetic engineering employs use of strong promoters before insertion of the gene of interest in a target organism.
Here, the lambda PE promoter seems to have low strength and weak binding. Thus, any gene placed post this promoter will be less expressed. Thus, the promoter region of lambda PE has been compared to the consensus and conserved sequence of the strong -35 element of strong promoters.
The λ PE promoter is known to have a weak promoter. Explain the reason for this...
1. Compare the structures of SO, to PF, and explain why they have different molecular shapes. (when comparing two objects, you should discuss both and mention both their similarities and differences and explain the reason for the differences) 1. Compare the structures of SO, to PF, and explain why they have different molecular shapes. (when comparing two objects, you should discuss both and mention both their similarities and differences and explain the reason for the differences)
Explain the reason why to have to know the spectrum of a communication signal?
1) What is the best reason that you have found to support physician-assisted suicide? Please explain your reasoning for considering this the best reason. 2) What is the best reason that you have found to oppose physician-assisted suicide? Please explain your reasoning for considering this the best reason. 3) Are there alternatives to physician-assisted suicide? Are any of these better options? Why or Why Not?
Which of the following isomers will have the highest boiling point? Explain the reason for your choice.
What is the best reason that you have found to support physician-assisted suicide? Please explain your reasoning for considering this the best reason.
Assume that ten years from now all registered nurses will have Bachelor's degrees. Explain one reason why you think this will change the status of nursing as an occupation and one reason why it won't change the occupation's status.
indicate whether it's true, false or uncertain and explain the
reason.
A.2 While we have lots of data on labour markets and the capital stock, we economists still need to rely on filters, like that proposed by Hodrick and Prescott, to calculate the business cycle.
3.13 pts) The restriction enzyme known as Notl recognizes the following sequence: 5-GCGGCCGC-3 3-CGCCGGCG-5 However, if the cytosines in this sequence have been methylated. NotI will not cleave the DNA at this site. For this reason, Net is commonly used to investigate the methylation state of CpG islands. A researcher has studied a gene, which we will call T. that is found in com, and encodes a transporter involved in the uptake of phosphate from the soil. A CpG island...
The Class C amplifier is known to have a Q-point below cutoff. Can you explain how this affects the performance of the amplifier?
Explain at least one possible reason why you might have the following results in an agarose gel electrophoresis of your PCR products. In addition to your DNA PCR sample, you also ran a Hi-Lo Marker, a positive PCR control, and a negative PCR control. 16. Scenario C: Your Hi-Lo marker showed up but there were no bands in the lanes for your PCR positive control, DNA PCR sample or negative PCR control.