Question

If I transfer 120 uL from a microcentrifuge tube with an initial dilution factor of 2.2...

If I transfer 120 uL from a microcentrifuge tube with an initial dilution factor of 2.2 x 10-3 into a second tube containing 1.23mL of water what is my final dilution factor (accounting for both dilutions)?

a.) 3.72 * 10-1

b.) 1.96 * 10^-4

c.) 3.02*10^-4

d.) 1.37*10^-1

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

dilution= aliqout volume/ final volume

aliqout volume= 120 uL

volume in the second tube= 1.23 mL

1 mL= 1000 uL

so 1.23 mL= 1.23\times1000= 1230 uL

final volume= 1230+ 120= 1350 uL

dilution= 120/1350=0.089

initial dilution factor of 2.2 x 10-3

final dilutionis the product of individual diliutions.

final dilution= 2.2 x 10-3 \times 0.089

= 1.955 \times 10^-4

so the answer is  b.) 1.96 * 10^-4

Add a comment
Know the answer?
Add Answer to:
If I transfer 120 uL from a microcentrifuge tube with an initial dilution factor of 2.2...
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
  • A student made an initial 1:5 dilution of protein lysate. Then 2mL of that was added...

    A student made an initial 1:5 dilution of protein lysate. Then 2mL of that was added to 8mL of water. Lastly, the student made a 1:20 dilution of the second tube. What is the final dilution of protein lysate 5. A student labeled 5 tubes 0, 1, 2, 3, 4, 5. Tube 0 contained undiluted protein lysate. The student used the tube 0 lysate to prepared 10-fold serial dilutions in the tubes labeled 1-5. What is the dilution of each...

  • 1) Well 1 contains 20 uL of serum. Wells 2-6 contain 90 uL of water. To...

    1) Well 1 contains 20 uL of serum. Wells 2-6 contain 90 uL of water. To do a serial dilution of 10% concentration (not volume) for each dilution, how many uL of liquid do you move between each well? ype your answer as a whole number of uL, but do not type the "uL" label. 2) Well 1 contains 20 uL of serum. Wells 2-6 contain 90 uL of water. What is the final concentration of well 6 if you...

  • dilutions dilutions What are the resulting dilutions? Notice units of measurement. a) b) c) 500 L...

    dilutions dilutions What are the resulting dilutions? Notice units of measurement. a) b) c) 500 L of serum is diluted to 2.0 mL 50 uL of whole blood is pipetted into 0.95 mL of diluent 500 mL of liquid K is added to 4.5 L of water 7. If 10 uL of urine is added to 90 uL of water, and the resulting solution is brought to a final volume of 0.50 mL with water, what is the final dilution...

  • Question 2 5 pts Transfer 0.1 mL of the bacterial suspension to the tube marked A1...

    Question 2 5 pts Transfer 0.1 mL of the bacterial suspension to the tube marked A1 (containing 0.9 mL of 0.1M MgSO4). Transfer 0.01 mL (10 PL) of the bacterial suspension from A1 to the tube marked A2 (containing 0.99 mL of 0.1M MgSO4). Transfer 0.01 mL of the bacterial suspension from A2 into the microcentrifuge tube marked A3 (containing 0.99 mL of 0.1M MgSO4). Close the lid, and mix. What is the dilution factor? A1 - 10x (1:10), A2-...

  • b. 1 ml 1ml 「-I Final dilution 4(1 point) This represents a serial dilution to determine...

    b. 1 ml 1ml 「-I Final dilution 4(1 point) This represents a serial dilution to determine viable bacterial counts. Indicate the final dilutions in each of the two tubes. Note that two different volumes of the cells intube #2 are plated onto agar plates A and B. Indicate the dilution factor that will be used to report the original cell concentration on a per mL basis. 1 ml 1 ml Final dilution in Tube #1 = Final dilution in Tube...

  • 1) Figure below show a 36 uL of stock solution containing 800 ppm of CuSO4 was...

    1) Figure below show a 36 uL of stock solution containing 800 ppm of CuSO4 was transferred into T1 tube contained with 324 uL of wash buffer. Next, serial dilution was performed from T1 to T5. (CuSO4 molar mass: 159.61 g/mol) 36 ul 120 ML 120 ML 120 L 120 L 800 ppm Cuso T1 Stock solution T2 T3 T4 TS B1 Dilution Factor Final Concentration NA 800 ppm Tube Volume Diluent Total Final Transferred Volume Volume Volume (PL) (wash...

  • .Viable plate count Using the formula: cfu/ml = (no. of colonies x dilution factor) / volume...

    .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...

  • For part 1 of this lab) I collected a soil sample from my campus Part 2)...

    For part 1 of this lab) I collected a soil sample from my campus Part 2) Tested bacteria initial viability Part 3) DNA extraction Part 4) DNA quantification by Nanodrop Part 5) Sample sequencing Part 6) PCR amplification Part 7) Gel electrophoresis Part 8) DNA sequence data analysis (sent sample to another lab) Directions for Part 3 DNA extraction are in the attached image QUESTIONS REGARDING PART 3 (DNA extraction) 1) What type of conclusions can be made from initially...

  • 1) How would you prepare 500mL of working TBE buffer if the stock solution was purchased...

    1) How would you prepare 500mL of working TBE buffer if the stock solution was purchased as 25X TBE? 2) 2mL of a serum sample was added to 18mL of phosphate buffered saline (PBS) in Tube 1. 10mL of Tube 1 was added to 40mL of PBS in Tube What is the dilution of serum in Tube 2? 3) A student needed to prepare 500mL of 1X TAE buffer to run a QC gel. The stock solution in the lab...

  • I just need the answers to questions 2 and 3. My DNA ladder is in lane...

    I just need the answers to questions 2 and 3. My DNA ladder is in lane 2 with the yellow arrow pointing to it. Thanks! Part 2: Gel purification and ration Gel Slice and PCR Product Preparation modified from IBSci.com instructions for gel and PCR clean-up system A. Dissolving the Gel Slice 1. Following electrophoresis, excise DNA band from gel and place gel slice in a 1.5ml microcentrifuge tube. 1b. Use an analytical balance to weigh gel slice. Record weight...

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