ive an example for any biopharmaceutical produced by Recombinant DNA Technology (except insulin). What is the name of the drug/trademark? Write its mode of action. List the experimental steps under the laborator

ive an example for any biopharmaceutical produced by Recombinant DNA Technology (except insulin). What is the name of the drug/trademark? Write its mode of action. List the experimental steps under the laborator

Complete Textbook Of Phlebotomy

5th Edition

ISBN:9781337464314

Author:Hoeltke

Publisher:Hoeltke

Chapter9: Sample Considerations And Special Procedures

Section: Chapter Questions

Problem 4.1E

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Give an example for any biopharmaceutical produced by Recombinant DNA Technology (except insulin).

What is the name of the drug/trademark?
Write its mode of action.
List the experimental steps under the laboratory conditions
List the production steps in the factory

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Give an example for any biopharmaceutical produced by Recombinant DNA Technology (except insulin). Answer option a,c,d a. What is the name of the drug/trademark?b. Write its mode of action.c. List the experimental steps under the laboratory conditionsd. List the production steps in the factory
Give an example for any biopharmaceutical produced by Recombinant DNA Technology (except insulin). Please take name of the drug/trademark is PROTROPIN. So, just answer 2,3,4 according to PROTROPIN What is the name of the drug/trademark? Write its mode of action. List the experimental steps under the laboratory conditions List the production steps in the factory
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Copy and paste the link below and watch the video on Youtube https://www.youtube.com/watch?v=8RBs0Ghg_48 Answer the following Questions: 1. What are the chemicals and materials used in gel electrophoresis? 2. Draw a schematic diagram of a gel electrophoresis set-up 3. Describe the procedure in doing a gel electrophoresis experiment. Why is there a need for a leveling bubble/leveler? What is the use of the rubber dam? 4. What is the use of ethidium bromide and why must you wear gloves when you handle it? 5. What makes the DNA fragment move towards the positive plate? 6. What is the purpose of glycerol in the sample buffer? 7. What is the use of a DNA ladder? 8. What will happen when you increase the voltage of the set-up? 9. Can gel electrophoresis be used to separate amino acids? If so, how is it done?