Question

Primers are short pieces of DNA that are used in PCR (Polymerase Chain Reaction), the process...

Primers are short pieces of DNA that are used in PCR (Polymerase Chain Reaction), the process which is used in molecular labs to make copies of short stretches of a gene or genome. You have designed primes that have a Molecular Weight (MW) of 6000. It arrives as a dry sample in the quantity of 300 µg. How much water do you need to add to make a primer stock solution of 100 mM primers?

HINTS: Remember that mM is a concentration; Molar (M) = moles / L

Break it down into steps.

1) The first step – how many mmol of primer do you have? (this requires you to use the MW)

2) How much water do you need to add to your mass (mmol) of primers to make a concentration of 100 mM?

0 0
Add a comment Improve this question Transcribed image text
Answer #1

2.

100mM= x nmoles of lyophilized primer+(x ×10microliter of molecular grade H2O.

300microgram =300000nanogram

300000nanogram of primer is added with 3000000microliter pcr grade water.it wil be 100mM

Add a comment
Know the answer?
Add Answer to:
Primers are short pieces of DNA that are used in PCR (Polymerase Chain Reaction), the process...
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. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Prepare a fragment of DNA to be cloned by PCR by preparing the oligonucleotides received through...

    Prepare a fragment of DNA to be cloned by PCR by preparing the oligonucleotides received through dilutions. The DNA to be used as a template is in a 50 ng/ul solution. The protocol is as follows: VOLUME TO ADD FINAL CONCENTRATION 0.5 UM 0.5 M REAGENT 10 PM Forward Primer 10 PM Reverse Primer Thermoestable pol Master mix 2x Template DNA water 1x 100 ng.. Total volume 25 ul Information about the primers: Forward primer: 29.3 nmoles - 220 ug...

  • Carolina Savirana Craz 3/12/20 GECC-Polymerase Chain Reaction 1. What is the purpose of the polymerase chain...

    Carolina Savirana Craz 3/12/20 GECC-Polymerase Chain Reaction 1. What is the purpose of the polymerase chain reaction? a. To repair damaged DNA b. To make copies of entire chromosomes c. To make copies of specific regions of DNA d. To prepare cells for cell division 2. The polymerase chain reaction is most comparable to what cellular process? a. Mitosis b. Replication c. Transcription d. Translation 3. When enzymes are elongating (building) a newly synthesized DNA strand in PCR, new nucleotides...

  • 2. You are performing PCR under the following conditions: 1. Each PCR reaction contains 50 pl...

    2. You are performing PCR under the following conditions: 1. Each PCR reaction contains 50 pl final volume II. Each PCR reaction contains: 1x PCR buffer, 1.5 mM MgCl2, 0.2 mM dNTP mix, 0.2 MM sense primer, 0.2 uM anti-sense primer, 1.5 units of Taq polymerase and 2 ul of DNA template. [all concentrations are final] III. Stock solutions of the following reagents are available: 10x PCR buffer, 25 mm MgCl2, 10 mM dNTP mix, 10 M of sense primer,...

  • After designig primers to target a gene of interest, you recieve 33.4 nmoles of a forward...

    After designig primers to target a gene of interest, you recieve 33.4 nmoles of a forward primer from the company. You want to make a 100uM stock but you accidentally made a 1mM stock solution. How much water do you need to add to your 1 mM stock to make it 100 uM?

  • qRT-PCR The reaction mixture for qRT-PCR requires the following: Taq Mix : 1 uL, SYBR Green...

    qRT-PCR The reaction mixture for qRT-PCR requires the following: Taq Mix : 1 uL, SYBR Green Mix: 25 uL, Forward primer : 1 uL, Reverse primer : 1 uL, ROX Reference Dye : 1 uL, Template : 50 ng RNA , Volume up to 50 uL with nuclease free water. If you are going to make a 20 uL reaction mixture and have a 10 ng/uL RNA sample, how much of each of the components do you need? You also...

  • 7. You are making a PCR reaction mixture with a total volume of 50uL.( THIS IS...

    7. You are making a PCR reaction mixture with a total volume of 50uL.( THIS IS IN MICROLITERS NOT MILILITERS AS ANOTHER QUESTION ON CHEGG HAS ALREADY BEEN POSTED BUT IT STATES THE TOTAL VOLUME AS 50 mL.) The primer set concentration is 1μl primer/10μl reaction volume. The plasmid stock solution concentration = 0.01μg/μl, of which you need 100ng. How much of each PCR reaction component will you add, given the following? 5x Mastermix __________ Primer set __________ DNA template...

  • D. After you run your PCR reaction, what next steps would you perform to determine that...

    D. After you run your PCR reaction, what next steps would you perform to determine that the PCR amplified the region of interest? E. After your procedures in step D above, you decide to measure the concentration of DNA in your PCR product. Briefly explain how you would do this given the tools we have available. What values would you expect to confirm that you have a good DNA concentration and purity? F. Write and briefly describe a program you...

  • Molecular Key Calculation - PLEASE NEED HELP TO CALCULATE IT! You are setting up you own...

    Molecular Key Calculation - PLEASE NEED HELP TO CALCULATE IT! You are setting up you own Master Mix for doing a Not1 restriction digest.              In each digestion tube you will be adding 10 ul DNA and 40 ul of your Master mix.              You are given 10 x Not1 buffer, 10 ug/ul acetylated BSA, Not1 restiction enzyme 10 units/ul and sterile water.              How much of each of the 4 reagents would you use to make 500 ul of...

  • For the PCR reaction you have to dilute the cDNA to 100 ng/µL. Your cDNA has...

    For the PCR reaction you have to dilute the cDNA to 100 ng/µL. Your cDNA has a concentration of 700 ng/µL. Taking 10 µL of this cDNA, by what factor to you have to dilute it and how much PCR water do you add?

  • Now. you should be able to answer the following questions: • How the amplification will be...

    Now. you should be able to answer the following questions: • How the amplification will be done? - How you will determine your target sequence? How the amplification will be specific for certain segment? What are the requirements to carry PCR? • Suppose you perform a PCR that begins with one double-strand of the following DNA template: +5'-CTACCTGCGGGTTGACTGCTACCTTCCCGGGATGCCCAAAATTCTCGAG-3+ +3'-GATGGACGCCCAACTGACGATGGAAGGGCCCTACGGGTTTTAAGAGCTC-5'+ A. Draw one cycle of PCR reaction below the following diagram. B. Label the template DNA, the primers, and what is...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT