How do we determine the best phage concentration to use to amplify our phage by the 10-plate method?
The 10-plate method is a series of serial dilution method by up to 10 times which helps in determining best phage concentration that amplifies the phage. It helps in counting and measuring the level of infection by the bacteriophages. This helps in measuring the ability of single infectious virus that is able to form the plaque. The plaque assay helps in tittering bacteriophage and helps in determining best phage concentration. It helps in visualizing the plaques when there is an actively growing population. The plaque define an initial infection as it leads to lysis of the bacteria that is close to it.
There is 10-fold dilution of the virus made for the plaque assay and after the incubation is over, the virus attach to the cell and grow on the nutrient medium. The infected cells are lysed and leads to release of the viral progeny. This leads to spreading of the new viruses to neighboring cells with each of the infectious cell producing plaque which is a circular zone. This helps in identifying the area or region where there is amplification of the viral bacteriophage.
How do we determine the best phage concentration to use to amplify our phage by the...
This week you’ll count plaques on your phage titer plates to determine the original phage titer in the tube we sampled from. Let’s say you counted 34 plaques on your clan’s “7” plate. Make a table or diagram that shows how many phage particles were in each tube of your dilution series.
How do we know if photosynthesis or cellular respiration is occurring in our experiment? How do we determine the progress in this experiment?(Hint: What would be the dependent variable(s) of our experiment?)
. If we increase the concentration of NaCl how will change the binding of our transcription factor to the DNA? How will change the melting point of DNA? Of course, explain.
Prepare the buffer. In this lab we store our buffer at a concentration 20 times the concentration used in the experiment. Thus we call it 20xLB. Before we can use it, it needs to be diluted to a 1x concentration. If we needed 20 mL of the media, we would take 1 mL of the 20xLB buffer and diluted it with 19 mL of Dl water. To make enough buffer for this experiment, we need 50 mL for the gel...
everything from how we use our credit cards to what we do on web sites. For the most part businesses and other organizations employ this data for useful purposes. However, as with most issues like this, a few bad actors who use the data for less-than-good and even criminal purposes spoil something that can be very helpful. If you were in charge, what rules and controls would you put in place in order to monitor and manage the use of...
We use data from the past to determine the best forecasting method for the future. What is one of the uses of this data from the past when dealing with selecting the best forecasting method? To determine the best value for c, the capacity of a water slide All the other answers are correct To determine the best weights for olympic lifting To determine the best value for alpha used in the forecasting method Exponential Smoothing
How do we balance the right to exercise our freedoms (that is, to do as we please), and the necessity to restrict those freedoms to protect society? Why?
How can we best enhance teacher preparation in our school systems today
how do you determine DNA/RNA purity, how do you determine DNA concentration, how do you determine protein concentration, and how do you determine cell density?).
2. G-proteins. How do G-proteins act as signal transducers and amplify a signal? 2. G-proteins. How do G-proteins act as signal transducers and amplify a signal?