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GA20OX Cloning Procedure and Analysis of Alpha-Amylase in Embryoless Seeds

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oralee
20 diapositives · 337 Views · Aug 10, 2014

This report outlines the GA20OX cloning procedure, focusing on the effects of gibberellins (GA) on alpha-amylase in embryoless seeds versus whole seeds. It addresses critical questions about treatment variations, absorbance measurements, and protein separation techniques. Furthermore, it delves into the SDS-PAGE process, detailing the steps involved in protein analysis, including sample preparation, gel formation, and protein transfer for detection. A detailed protocol ensures clarity in experimental procedures and troubleshooting methods.

#ga20ox cloning procedure and analysis of alpha-amylase in embryoless seeds #ga20ox cloning procedure and analysis of alpha-amylase in embryoless seeds ppt #powerpoint #presentation
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GA20OX Cloning Procedure and Analysis of Alpha-Amylase in Embryoless Seeds
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  1. Report • Draw a scheme of the GA20OX cloning procedure.

  2. Question 1: Why do we study the effect of GA on alapha-amylase in embryoless seeds and not on whole seeds? Question 2: Volumes Question 3: Why do we do treatment 4? What is the difference to treatment 3? Question 4: What is the "debris"? Question 5: Why is the decrease in absorbance proportional to the quantity of alpha-amylase in the reaction mixture? Question 6: What do you do if your absorbance in your extract is out of the range of your standard curve?

  3. Western Blot

  4. Steps: 1. SDS-PAGE 2. Transfer to membrane: "Blotting" 3. Detection of proteins

  5. SDS-PAGE SDS: sodium dodecyl sulfate PAGE: polyacrylamid electrophoresis

  6. The goal is to separate proteins according to their sizes. How would you do that?

  7. Remember

  8. SDS: sodium dodecyl sulfate is a detergent (soap) that can dissolve hydrophobic molecules but also has a negative charge (sulfATE) attached to it http://www.davidson.edu/academic/biology/courses/Molbio/SDSPAGE/SDSPAGE.html

  9. www.ufs.ac.za

  10. Reductant: DTT: Dithiothreitol B-Mercaptoethanol The reducing agent beaks any cystine (-S-S-) bonds formed between two cysteine residues

  11. Other stuff in the sample buffer: Glycerol Bromphenolblue

  12. How to make the gel?

  13. Polymerization reaction: radical catalyzed reaction http://www.davidson.edu/academic/biology/courses/Molbio/SDSPAGE/SDSPAGE.html

  14. Polymerization reaction Catalysts: APS: Ammonium persulfate, radical initiator TEMED:N, N, N', N'-tetramethylethylenediamine, free radical stabilizer http://www.davidson.edu/academic/biology/courses/Molbio/SDSPAGE/SDSPAGE.html

  15. "Discontinuous" PAGE Low pH (6.8) Low ionic strength Low Acrylamid concentration FAST High pH (8.8) High ionic strength High Acrylamid concentration SLOW

  16. Visualization of proteins on the gel: Coomasie stain

  17. OR do a western blot Proteins are transferred to a protein binding membrane. We will use a nitrocellulose membrane. Polyvinylidene difluoride (PVDF) is also commonly used.

  18. OR do a western blot