Laboratory Calculations Problem Help (2024)

  1. If 10x TBE contains 0.89 M Tris-borate, 0.89 M Boric acid, and 0.02 MEDTA, what is the Molar concentration of Tris-borate in 100 ml of 1x TBE?
    • Since molar concentrations are an expression of the molecular weight perliter, the fact that the question asks for 100 ml is irrelevant. Whether youare dealing with 1000 ml, 100 ml or 10 ml, the Molar concentration will be thesame. What is important is the change from 10x to 1x.
    • Since the concentration, 10x is divided by 10 to arrive at a 1xconcentration, then the Molar concentration is also divided by 10.
    • The concentration of Tris-borate in 100 ml of 1x TBE is 0.089 M.
  2. How many ml of 0.5 M EDTA are required to make 100 ml of a 0.1 M EDTAsolution?
    • Remember: initial concentration x initial volume = final concentration xfinal volume
    • (0.5 M) (X ml) = (0.1 M) (100 ml)
    • (X ml) = (0.1 M) (100 ml) / (0.5 ml)
    • X ml = 20 ml of 0.5 M EDTA
  3. If a solution of DNA is 3 mg/ml, 0.5 mg of DNA would be contained in howmany ml?
    • This can be set up as a simple proportion
    • 3 mg/ 1 ml = 0.5 mg/ X ml
    • (3 mg) (X ml)/ 1 ml = 0.5 mg
    • (3 mg) (X ml) = (0.5 mg) (1 ml)
    • X ml = (0.5 mg) (1 ml)/3 mg
    • X ml = 0.17 ml
    • 0.5 mg of DNA would be contained in 0.17 ml of the 3mg/ml solution
  4. If you have a 5x stock solution, how much of this stock would be needed tomake 100 ml of a 1x solution? 10 ml of a 1x solution? 33 ml of a 1x solution?
    • initial concentration x initial volume = final concentration x final volume
    • For 100 ml:
    • (5x) (X ml) = (1x) (100 ml)
    • X ml = (1x) (100 ml)/(5x)
    • X ml = 20 ml of a 5x
    • For 10 ml:
    • (5x) (X ml) = (1x) (10 ml)
    • X ml = (1x) (10 ml)/(5x)
    • X ml = 2 ml of a 5x
    • For 33 ml:
    • (5x) (X ml) = (1x) (33 ml)
    • X ml = (1x) (33 ml)/(5x)
    • X ml = 6.6 ml of a 5x
  5. How many grams of agarose are needed to make 100 ml of a 2% agarosesolution?
    • This is a weight to volume equation so remember:
    • g % means the number of grams in 100 ml.
    • 2% is 2 g in 100 ml of diluent.
  6. How many ml of the detergent Nonidet P-40 would be used to make 43 ml of a7 % detergent solution?
    • This is a volume to volume conversion so use:
    • initial concentration x initial volume = final concentration x final volume
    • (100 %) (X ml) = (7 %) (43 ml)
    • X ml = (7 %) (43 ml)/ 100 %
    • X ml = 3.01 ml of Nonidet P-40
  7. An extraction buffer for DNA is stored as a 15x stock solution. How muchof this stock solution would be required to make 7.5 ml of a 1x workingsolution? a 0.5x solution?
    • initial concentration x initial volume = final concentration x final volume
    • For a 1x working solution:
    • (15x) (X ml) = (1x) (7.5 ml)
    • X ml = (1x) (7.5 ml)/ 15x
    • X ml = 0.5 ml of the 15x solution
    • For a 0.5x solution:
    • (15x) (X ml) = (0.5x) (7.5 ml)
    • X ml = (0.5x) (7.5 ml)/ 15x
    • X ml = 0.25 ml of the 15x solution
  8. Given the following stock solutions: 1 M Tris, 0.5 M EDTA, 4 M NaCl, dothe calculations necessary to make 1 L of a solution containing 100 mM Tris, 100mM EDTA, 250 mM NaCl.
    • The information needed to complete this problem includes calculating thevolume of each of the stocks required then the volume of diluent required toreach the final volume.
    • First, convert the units so you are working in similar units
    • Second, use
    • initial concentration x initial volume = final concentration x final volume
    • to determine each of the volumes of stocks to be used
    • For Tris:
    • (1000 mM ) (X ml) = (100 mM) (1000 ml)
    • X ml = (100 mM) (1000 ml)/ 1000 mM
    • X ml = 100 ml of 1 M Tris
    • For EDTA:
    • (500 mM) (X ml) = (100 mM) (1000 ml)
    • X ml = (100 mM) (1000 ml)/ 500 mM
    • X ml = 200 ml of 0.5 M EDTA
    • For NaCl:
    • (4000 mM) (X ml) = (250 mM) (1000 ml)
    • X ml = (250 mM) (1000 ml)/ 4000 mM
    • X ml = 62.5 ml of 4 M NaCl
    • Before calculating the amount of diluent needed, you must know what is thecombined volume of all of the initial dilutions
    • 100 ml Tris + 200 ml EDTA + 62.5 ml NaCl = 362.5 ml This is the totalamount of initial volumes to be used.
    • Finally use
    • final volume - combined initial volumes = diluent
    • to find the amount of diluent needed to bring the final volume to 1000 ml.
    • 1000 ml - 362.5 ml = 637.5 ml of diluent
  9. How many ml of a 1 x 10Laboratory Calculations Problem Help (1) cells/mlsuspension should be used to plate out 500 cells/plate? 100cells/plate?
    • All that is being asked in this problem is to determine the volume whichcontains the number of cells needed. A simple proportion will work here.
    • The volume which contains 500 cells would be:
    • 1 x 10Laboratory Calculations Problem Help (2) / 1 ml =500 / X ml
    • X ml = (500) (1 ml) / 1 x 10Laboratory Calculations Problem Help (3)
    • X ml = 0.0005 ml would contain 500 cells
    • The volume which contains 100 cells would be:
    • 1 x 10Laboratory Calculations Problem Help (4) / 1 ml =100 / X ml
    • X ml = (100) (1 ml) / 1 x 10Laboratory Calculations Problem Help (5)
    • X ml = 0.0001 ml would contain 100 cells
  10. The following stock solutions are available to make a protein extractionbuffer: 100% Nonidet P-40, 1 M Tris-Cl, and 0.5 M EDTA. What quantity of theoriginal stocks will be needed to make 250 ml of buffer with the following finalconcentrations: 0.5% Nonidet, 150 mM Tris-Cl, and 10 mM EDTA?
    • This should be done in the same manner as Problem number 8.
    • For Nonidet P-40:
    • (100 %) (X ml) = (0.5 %) (250 ml)
    • X ml = (0.5 %) (250 ml)/ 100 %
    • X ml = 1.25 ml of Nonidet P-40
    • For Tris-Cl:
    • (1000 mM) (X ml) = (150 mM) (250 ml)
    • X ml = (150 mM) (250 ml) / 1000 mM
    • X ml = 37.5 ml of Tris-Cl
    • For EDTA:
    • (500 mM) (X ml) = (10 mM) (250 ml)
    • X ml = (10 mM) (250 ml) / 500 mM
    • X ml = 5 ml of
    • 1.25 ml + 37.5 ml + 5 ml = 43.75 mlcombined initial volumes
    • 250 ml - 43.75 ml = 206.25 ml of diluent are needed

Serial Dilution Problems

Thanks are given to the MMG graduate students for suggesting these problems.

Laboratory Calculations Problem Help (6)Laboratory Calculations Problem Help (7)Laboratory Calculations Problem Help (8)

©The University of Vermont

As an expert in molecular biology and laboratory techniques, I have substantial experience and knowledge in various concepts related to solutions, concentrations, dilutions, and calculations typically encountered in molecular biology experiments.

Let's dissect and elaborate on the concepts used in the provided article to solve different scenarios related to solutions, concentrations, and dilutions:

  1. 10x TBE Solution:

    • Defined components: 0.89 M Tris-borate, 0.89 M Boric acid, and 0.02 M EDTA.
    • Conversion from 10x to 1x concentration: Involves dividing the concentrations by 10.
  2. Calculating Volumes for Desired Concentrations:

    • Determining volumes to create desired molarities: Utilizing the formula initial concentration × initial volume = final concentration × final volume.
  3. Calculations Involving Known Concentrations:

    • Given initial concentrations and final volumes, calculating the required volumes of stock solutions or diluent needed to achieve specific concentrations in a final solution.
  4. Agarose Solution Preparation:

    • Understanding percentage (weight/volume) calculations to prepare a solution of a given concentration.
  5. Determining Volume from Percentage:

    • Calculating volumes based on given percentages and final volumes for a particular solution, as in the case of detergent solutions.
  6. Serial Dilution Problems:

    • Solving problems involving serial dilutions to achieve desired concentrations using initial concentrations and final volumes.
  7. Cell Count and Volume Calculations:

    • Relating cell count per volume to determine the volume needed for specific cell counts.
  8. Multiple Stock Solutions to Achieve a Final Buffer:

    • Utilizing multiple stock solutions to create a buffer with specified final concentrations, employing the concept of solving for individual volumes required for each component.

These concepts collectively cover a wide array of scenarios encountered in molecular biology laboratories, including the preparation of solutions, dilutions, and calculations involving concentrations and volumes for experiments involving DNA, protein extraction, cell culture, and buffer preparations.

If you have any specific questions or need further explanations regarding these concepts or any related queries in molecular biology or laboratory techniques, feel free to ask!

Laboratory Calculations Problem Help (2024)

FAQs

How to do laboratory calculations? ›

Just plug the values into the formula:
  1. (initial concentration)(initial volume) = (final concentration)(final volume)
  2. (4 µg/µl)(10 µl) = (X µg/µl)(50 µl)
  3. X µg/µl = (4 µg/µl)(10 µl) / 50 µl.
  4. X µg/µl = 0.8 µg/µl.

How to include calculations in a lab report? ›

Clearly label each type of calculation, by indicating what quantity you are calculating. Your instructor may tell you to include your sample calculations at the end of your lab report, in a separate section called an APPENDIX. If this is the case, label all appendices sequentially (Appendix 1, Appendix 2, etc.).

How to convert 10x to 1x? ›

Answer and Explanation: To make 1 liter of 1x buffer, measure 100 mL of 10x stock and add 900 mL water to make the total volume equal to 1000 mL (1 liter). This is a 1:10 dilution.

How to calculate 10x buffer? ›

To calculate the amount of sample loading buffer, you can use the dilution equation: C1V1 = C2V2, where C1 is the initial concentration, V1 is the initial volume, C2 is the final concentration (10x), and V2 is the final volume (100 µl).

How do you master pharmaceutical calculations? ›

How to Pass Any Pharmacy Calculation Exam!
  1. Don't rush. ...
  2. Time yourself. ...
  3. Identify loaded information. ...
  4. Know units, conversions, and formulae. ...
  5. Verifying your answers. ...
  6. Arrive to the exam on-time. ...
  7. Optimize study time.

What is a sample calculation in a lab? ›

OBJECTIVE The objective of the Sample Calculations is to document how the experimental results have been calculated from the raw data. Well presented sample calculations will establish the author's credibility with the reader.

What are the 7 steps of a lab report? ›

It is usual to write your report under a set sequence of sub-headings such as, for example:
  • Introduction. Explain why you did the experiment, identify what were your goals and describe the factors that you considered.
  • Materials and methods. ...
  • Observations and results. ...
  • Analysis. ...
  • Conclusions. ...
  • Note.

How do you dilute 500X to 1X? ›

For example: A stock solution that is 500 times more concentration would be written as 500X and would require a 1:500 dilution to restore the normal working concentration. Therefore, to make a 1X working solution you would need to add 2 µL of your stock solution into 1 mL of a buffer of your choice.

How to convert 20X to 1X? ›

So, we need 50mL of 20X SB to make 1L of 1X SB. Measure 50mL of 20X SB, then bring it up to volume (1000mL) by adding 950mL of distilled water. 1 liter of 1X SB buffer is enough to run gels for labs 1.2 and 4 (or 4a) for two lab groups.

What is a 20X solution? ›

A solution 20 times more concentrated would be denoted as 20x and would require a 1:20 dilution to restore the typical working concentration. Example: A 1x solution of a compound has a molar concentration of 0.05 M for its typical use in a lab procedure.

How do you convert 10X PBS to 1X? ›

By preparing 10x instead of 1x PBS solution, you can dilute 100ml of the 10X solution to 900ml of distilled water to obtain 1l of 1x PBS buffer.

What does 10X mean in lab? ›

Concentrated solutions can be expressed in terms of fold-concentrated. If a standard, final concentration is termed 1X (1 fold concentrated), a solution concentrated ten-fold is termed 10X. A 1X solution can be made from a 10X solution be diluting the 10X solution ten-fold.

How is 10X calculated? ›

Obviously, the way to calculate a return multiple is to divide the amount returned from an investment by the dollars invested. If I invested $10M in a company and got back $100M, that's a 10X return.

How do you do chemical calculations? ›

To calculate it, one needs to divide the mass of each element in a molecule by the total molecular mass and then multiply by 100%. This calculation gives the contribution of each element to the overall mass of the molecule and is often used to determine the empirical formula or assess the purity of a compound.

How do you calculate drug calculations? ›

How to calculate drug dosage per kg
  1. Determine the dosage of the drug. ...
  2. Weigh the patient in kg.
  3. Multiply the dosage by the patient's weight.
  4. Divide the dosage by the number of times the patient will take the drug in the day. ...
  5. If the drug is in liquid form, it will have a concentration.

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