Question

The A260nm of a DNA solution is 0.12. How much of this DNA solution and a...

The A260nm of a DNA solution is 0.12. How much of this DNA solution and a 5.5X loading dye should you add to 15µL of water to obtain a sample which contains 30ng of DNA in 0.5X loading dye? (A260nm of 1.0 = 50 µg/mL DNA)

Answer is 5µL DNA and 2µL dye, please show work

Homework Answers

Answer #1

Let

y ul of DNA and z ul of dye is added to 15 ul of water

so

final volume = 15 + y + z

now

consider the loading dye

we know that

during dilution

M1V1 = M2V2

so

5.5 x z = 0.5 x ( 15 + y + z)

5.5z = 7.5 + 0.5 y + 0.5z

5z = 7.5 + 0.5y


given

1.0 = 50 ug / ml DNA

so

0.12 = 6 ug / ml DNA = 6 ug / 1000 uL DNA

0.12 = 0.006 ug / uL DNA

now

given

amount of DNA = 30 ng = 0.03 ug

so

0.03 / y = 0.006

y = 5

now

5z = 7.5 + 0.5 y

so

5z = 7.5 + 2.5

z =2

so

5 ul of DNA and 2 ul of dye should be taken

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
When adding your DNA samples to the agarose gel, you will need to add loading dye...
When adding your DNA samples to the agarose gel, you will need to add loading dye to the samples. Loading dye contains: ¥ glycerol, which helps the samples sink into the sample wells of the gel; and ¥ tracking dyes so that you have a way of estimating how far the samples have travelled through the gel during electrophoresis. The recipe for 6X loading dye is as follows: ¥ 0.25% bromophenol blue (w/v) ¥ 0.25% xylene cyanol (w/v) ¥ 30%...
How much water should you add to 51.5 mL of a 3.25 M iron (III) chloride,...
How much water should you add to 51.5 mL of a 3.25 M iron (III) chloride, FeCl3, stock solution to make a 1.70 M solution? A) 9.32 mL B) 98.5 mL C) 47.0 mL D) 27.0 mL E) 24.6 mL *explain why answer B is wrong, please show steps to getting right answer, do not use m1*v1=m2*v2 Thank you
Determining Conc. of DNA: A260 of 1.0 = 50µg/mL or 50ng/µL Question: A DNA sample is...
Determining Conc. of DNA: A260 of 1.0 = 50µg/mL or 50ng/µL Question: A DNA sample is at a concentration of 250ng/100µL. What would be the absorbance at 260nm of a 1/2.5 dilution of this DNA sample? Answer is 0.02, please show all steps of how we got this answer
1)You are given a protein solution with a concentration of 0.15 mg/ml. We need 10 µg...
1)You are given a protein solution with a concentration of 0.15 mg/ml. We need 10 µg for an experiment. What volume of the protein solution do we need? My answer: Convert 0.15 mg/ml to μg/ μl and you will get 150 μg/ μl. C = M/V rearrange for Volume V= M/C , V= (10 μg)/(150 μg/ μl) = 0.06667 μg/ μl 2) Suppose we want to prepare a solution containing 100 µg of the protein at a concentration of 1...
You had a total of 1.0 mL of "transformation mixture" including the cells and DNA. How...
You had a total of 1.0 mL of "transformation mixture" including the cells and DNA. How many TOTAL transformants would you have seen if you had plated the whole 1 mL of transformed cells? (There are many ways to approach this questio, given your numbers above) . Please explain you reasoning. Below are the number of transformants I counted for each plate. There are two plates of each 25, 50 and 100 microliter. 25 microliters plated: 249, 186 50 microliters...
A lab group needs to determine the concentration of DNA in their PCR product. The 500bp...
A lab group needs to determine the concentration of DNA in their PCR product. The 500bp band of the SS (DNA Size Standard) on a gel contains 50ng of DNA. The lab group loaded 10ul of PCR product + 5ul of Blue Juice Dye which resulted in a band 3 times as bright as DNA SS. A.) How many ng of DNA is in their PCR product? B.) What is the concentration of their PCR product (ng/ul)? C.) If the...
Please answer all parts if possible: Describe how to prepare a 20.00 µg/mL iron solution from...
Please answer all parts if possible: Describe how to prepare a 20.00 µg/mL iron solution from a 1 000 mg/mL iron standard solution using 10-mL and 50-mL volumetric pipets and 500-mL and 1 000-mL volumetric flasks. Accounting for buoyancy, what APPARENT mass of CsCl (density = 3.988 g/mL) in air should you weigh out to obtain a TRUE mass of 1.267g? Part B: By using the ideal (perfect) gas law (PV = nRT), calculate the density of He at 20...
Your new <$1 million grant has afforded you the ability to isolate DNA from bacterial cells....
Your new <$1 million grant has afforded you the ability to isolate DNA from bacterial cells. You want to estimate how much DNA is present in your sample. You use 30 µL of sample, add 270 µL of buffer, and receive an A260 of 0.40 and A280 of 0.25. (You can use whichever method you prefer on (a) and (b), but be consistent for both. a. (2 pt) Assuming the sample was pure, about how much double-stranded DNA was present...
You’ve been asked to prepare the gel. How much agarose would you need to weigh in...
You’ve been asked to prepare the gel. How much agarose would you need to weigh in order to prepare 50 ml of 2% gel? Show your math. List three things to which one needs to pay special attention when loading a gel for DNA electrophoresis. What would be the volume of the PCR sample you would have loaded in live lab? The loading buffer has a dual purpose. Explain. There are multiple reasons for loading a DNA ladder (size standard)...
given the initial and final ph. how do you determine how much of a strong acid...
given the initial and final ph. how do you determine how much of a strong acid to add to water to obtain the final ph. given intial ph = 4 final ph = 7 volume of water = 10 liters concentration of strong acid (HCL)= 3 moles/L So how much HCl (in mL) do we have to add to water to obtain the final ph of 4