Question

In: Biology

You have thoroughly mixed 10 million cells in 10 mL of tissue culture medium to be...

You have thoroughly mixed 10 million cells in 10 mL of tissue culture medium to be plated in 96 wells of a microliter plates, delivering 100 microliters per well.

a. What is the probability that a well will have no cells in it?

b. What is the probability that a well have one cell?

c. What is the probability that a well will have 3 cells or more?

Solutions

Expert Solution

Answer:

Based on the given information:

  • Total number of wells = 96
  • Total volume of media (containing cells) used for delivering in 96-well plate = 96 *100ul = 9600ul (9.6ml)
  • Concentration of cells = 10 million cells / 10ml = 1 million cells / ml = 106 cells/ml = = 106 cells/1000ul
  • Volume delivered in 96-well microtiter plate (per well) = 100ul
  • Average number of cells in a single well of microtiter plate = 106 / 10 = 105 cells / well
  • The distribution of cells follows a poisson distribution.

a. What is the probability that a well will have no cells in it? b. What is the probability that a well have one cell?

Since the tissue culture medium is thoroughly mixed, therefore each well is expected to contain around 100000cells. The probability that a well will have no cells or one cell in it is close to 0.

c. What is the probability that a well will have 3 cells or more?

  • The probability that a well will have 3 cells or more will be close to 1.

Related Solutions

Tissue culture medium is the “soup” that cells are grown in. Briefly describe its composition and best conditions for cell culturing.
Tissue culture medium is the “soup” that cells are grown in. Briefly describe its composition and best conditions for cell culturing. (Hint: List the names and write down for what purpose we use them)?
How would you prepare adherence cells (tissue culture) in a flow cytometry?
How would you prepare adherence cells (tissue culture) in a flow cytometry?
You think you have a culture of Streptococcus pyogenes, but you may have mixed it up...
You think you have a culture of Streptococcus pyogenes, but you may have mixed it up with another Gram-positive organism. By referring to the flow chart in this exercise, list in order the two tests you should do to confirm that the culture is in factStreptococcus pyogenes, AND explain what the correct result should look like for both tests.
2. After your frustration with tissue culture, you finally get your cells passaged and decide to...
2. After your frustration with tissue culture, you finally get your cells passaged and decide to set up your cDNA synthesis reaction, PCR, and agarose gel. You have extracted RNA from your cells, and now you need to proceed with the cDNA synthesis. a. The first step is to determine the concentration of your RNA. You dilute your RNA 1:250, vortex it, move it to the cuvette, and run it on the spectrophotometer.   The spec tells you that your concentration...
10 mL of 10% calcium chloride injection and 10 mL ofmultivitamin infusion are mixed with...
10 mL of 10% calcium chloride injection and 10 mL of multivitamin infusion are mixed with 500 mL of a 5% dextrose injection. The infusion is to be administered over 5 hours. If the dropper in the set calibrates 15 drops/mL, at what rate, in drops per minute, should the flow be adjusted to administer the infusion over the desired time interval? Round to nearest whole number.
You are given a vial of cells at a density of 6.8 x 10^6 cells/ml. You...
You are given a vial of cells at a density of 6.8 x 10^6 cells/ml. You are asked to seed a 12 well plate, which requires 2 x 10^5 cells per well. Because every well requires a final media volume of 1mL, your professor asks you to dilute your cells with media so that you can directly add 1ml of diluted cells per well in the plate. How you would dilute your cells so that each well receives 2 x...
Using a luciferase reporter system in tissue culture cells, researchers from the University of California, San...
Using a luciferase reporter system in tissue culture cells, researchers from the University of California, San Francisco, found that ethanol stimulates transcription of genes in brain cells possibly involved in adaptive responses to alcohol. This process was found to depend on PKA activation. By analogy to other PKA-dependent transcription activation pathways, describe a possible pathway for this transcription induction. What other proteins would be involved?
You have been employed by a wholesale nursery to set up a new plant tissue culture...
You have been employed by a wholesale nursery to set up a new plant tissue culture facility to propagate selected desirable cultivars of ornamental orchids. The nursery has allocated a maximum of $AUD10,000 for you to purchase the necessary materials, and has requested that you prepare a report to the manager for consideration.   1. What are the materials needed to set up the facility? (E.g. large equipment, small equipment (glassware etc), consumables (hormones, medium etc) etc)
You have 100. mL of aqueous 0.40 M CuSO4 mixed with 100. mL of aqueous 0.20...
You have 100. mL of aqueous 0.40 M CuSO4 mixed with 100. mL of aqueous 0.20 M Na2S. 1. What kind of reaction could potentially take place? (a) Bronsted-Lowry acid base (b) redox (c) precipitation (d) no reaction 2. Which of the following is/are the spectator ions in this reaction? (a) SO42-   (b) Na+ (c) S2- (d) Cu2+ 3. After the solutions are mixed, what will be the concentration of Na+ ? (a) 0.10M (b) 0.80M (c) 0.20M (d) 0.40M...
1) If you suspect your culture of bacteria has 125 x 106 cells per mL, what...
1) If you suspect your culture of bacteria has 125 x 106 cells per mL, what would you want the final dilution to be in order to end up with 50 cfu on a plate? 2) A 0.1 dilution is performed on a culture of bacteria in order to perform viable plate counts. From the dilution, *0.1 mL* of solution is plated on solid media, and 154 colony forming units grow on the plate. How many bacteria are in a...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT