1. We need 400 mL of 1X TBE (Tris-Boric Acid- EDTA) buffer to run a DNA gel. Melina has a 10X TBE stock prepared. How would you prepare enough for one gel? For a class that has 8 groups (8 gels)?
1. We need 400 mL of 1X TBE (Tris-Boric Acid- EDTA) buffer to run a DNA gel. Melina has a 10X TBE stock prepared. How would you prepare enough for one gel? For a class that has 8 groups (8 gels)?
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![1. We need 400 mL of 1X TBE (Tris-Boric Acid- EDTA) buffer to run a DNA gel. Melina
has a 10X TBE stock prepared.
How would you prepare enough for one gel? For a class that has 8 groups (8 gels)?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F6746fa6f-1856-443b-addc-ecae5d9da9b9%2Fa1a37c45-955c-43bf-8b54-af3f91f5ce2d%2Fsxb04h_processed.jpeg&w=3840&q=75)
Transcribed Image Text:1. We need 400 mL of 1X TBE (Tris-Boric Acid- EDTA) buffer to run a DNA gel. Melina
has a 10X TBE stock prepared.
How would you prepare enough for one gel? For a class that has 8 groups (8 gels)?
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