Dilution factor = Volume of resulting solution (milk +diluent)/ volume of milk
First dilution
1 ml of milk was diluted into 99 ml of diluent = so 1 ml of milk in 100 ml of resulting solution
Dilution factor 100/1= 102
Second dilution
0.1 ml of the diluted solution is mixed with 0.9 ml of diluent. so 0.1 ml of diluted milk in 10 ml of resulting solution
Dilution factor = (initial dilution factor) X 10/0.1 = 102 X 102 = 10 4
Answer E) 10 4
A student set up a standard plate count on a sample of milk in the following...
may you help me figure out how to solve 7-9
Standard plate count. Include formulas and calculations. Scientific notation. Show your work. UNITSI 7. Suppose you have 2.0 ml of an undiluted E.coli broth and need to begin your serial dilution by making a 10. solution. How much diluent would you need if you wanted to use the entire 2 ml of E. coli broth? 110-ml 102 = 2mL ol os dition 10 8. If you transfer 0.1 ml of...
Problem solving Question: 1. If you were to serially dilute a sample with three 1:10 dilutions, what would be the final dilution of the last tube? 2. If you add 1 ml of sample to 99 ml of water, and then add 0.1ml (100pl) to the agar plate what is the dilution of the sample on the plate? 3. If you count 98 colonies on the 10-5 plate, how many bacteria/ml were in your sample? 4. What are three ways...
.Viable plate count Using the formula: cfu/ml = (no. of colonies x dilution factor) / volume of culture plate In plate 10-4 there were 150 colonies counted. Experimental process: Pipet 0.25 mL of the S. cerevisiae solution into the test tube labeled 10-1. Pipet the solution up and down several times to ensure all organisms are rinsed from the pipet into the test tube. Pipet 0.25 mL of the 10-1 S. cerevisiae solution into the test tube labeled 10-2. Pipet...
your lab manual for instructions, Sample plated Number of colonies on plate TMTC 430 4th plate 5th plate 6th plate 75 Which plate has the countable number of colonies? What is the dilution factor that produced that plate? • What is the correction factor for the volume? How many cfu/ml are in the culture, based on your calculations? 4. Suppose you plated 1 ml of a 10-7 dilution (tenfold dilutions) of a bacterial broth culture
In order to count cells, the culture must be duted The technique o serialul precise and quantitative method alle e n al b e performed allow you to determine how many well per miller were the time the were made in overview knowvolume of culturedded to know Volume 0 sterile diluent aliquid that will not harm the cell The liquid in this tube is mixed and known volume of this culture is transferred to another known volume of sterile diluent...
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m e usually performed, e.g., 10°>10% 10% 10%, etc. Two-fold or other dilution schemes can be applied as well. For accurate quantitation, it is important to use the selected dilution scheme consistently. correction factor is 10 (0.1 ml X 10-10 ml). If you plated 0.5 ml, the correction factor is 2. 1.-CFU/Dr Initial concentration, (lc) equals colony forming units (cfu) divided by dilution factor (Df). Note that each step of the dilution procedure reduces the...
Write the formula for calculating the CFU/ml here and put in the numbers used. CFU (Colony Forming unit) CFU/ml= (Number of Colonies|Dilution factor) (Volume of culture plate) Conclusion: In a narrative form Using the 51 (Chapter 3, Cowan lecture book) Inoculation agar, Incubation, Isolation, Inspection, Identification Use the 5 l-s to explain how it was decided that the infectious southe was or was not the cause The number of colonies in first plate is 79. The number of colonies in...
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Name One use of serial dilutions is to calculate the concentration of microorganisms. Since it would usually be challenging or even impossible to actually count the number of microorganisms in a sample, the sample is diluted and plated to get a reasonable number of colonies to count (usually between 25 to 250 colonies is the goal). Since each colony on an agar plate theoretically grew from a single microorganism,...
1. On a serial dilution with the following tubes set up, 1:2, 1:4, 1:8, 1:16, 1:32, and 1:64, there is no visible agglutination in the 1:64 tube. What is the titer of the antibody? A. 32 B. 16 C. 64 D. Cannot be determined 2. If you want to make 2 mL of a 1:20 dilution, how much serum would be needed? 3. When 1.0 mL of serum is added to 3.0 mL of diluent, what dilution does this represent?...
A microbiology student was carrying out an independent research
project in which he needed to know the number of infectious phage
particles added during a particular step in an experimental
protocol. In preparation for the experiment, he passed a crude
mixture of phage plus infected bacteria through a 0.45 micrometer
filter and collected the filtrate (portrayed below in the
green-capped Eppendorf tube):
Once the filtrate was prepared, the student used the P-20 shown
in the photograph to transfer a volume...