GMU:DIY Biolab “Driver’s License”/Marie Laure Ebel: Difference between revisions

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==HUMAN DNA ANALYSIS==
==HUMAN DNA ANALYSIS==


I grew up with the fantasy that I must have something exotic deep inside me. People frequently asked me about my relatives, and I started to believe that I somehow belong to another soil than my motherland. Having the chance to work in a DIY Biolab, I decided to pursue my intersect feelings and I attended to analyze my DNA sequences, with the secret hope of discovering my own ethnicity extent and finding any connection with Asian pattern genome.
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File:Blood collected2.jpg|Blood collected2
File:Blood collected2.jpg|Blood collected2

Revision as of 13:02, 30 January 2018

HUMAN DNA ANALYSIS

I grew up with the fantasy that I must have something exotic deep inside me. People frequently asked me about my relatives, and I started to believe that I somehow belong to another soil than my motherland. Having the chance to work in a DIY Biolab, I decided to pursue my intersect feelings and I attended to analyze my DNA sequences, with the secret hope of discovering my own ethnicity extent and finding any connection with Asian pattern genome.

PRACTICING PCR ANALYSIS

Step 1. Extracting DNA from blood and from pork liver meat

STEP 1.1.jpg STEP 1.2.jpg STEP 1.3.jpg STEP 1.4.jpg STEP 1.5.jpg STEP 1.6.jpg STEP 1.7.jpg STEP 1.8.jpg STEP 1.9.jpg STEP 1.10.jpg STEP 1.11.jpg


Step 2. STR-analysis with pork meat primer

STEP 2.1.jpg STEP 2.2.jpg STEP 2.3.jpg STEP 2.4.jpg STEP 2.5.jpg STEP 2.6.jpg STEP 2.7.jpg


Step 3. Electrophoresis

#First attempt

STEP 3.1.JPG STEP 3.2.JPG STEP 3.3.JPG STEP 3.4.jpg STEP 3.5.jpg STEP 3.6.jpg STEP 3.7.JPG STEP 3.8.JPG STEP 3.9.JPG STEP 3.10.JPG

=> I got no results : either the ladder nor the DNA samples were "growing" as they should (multiple lines). So I decided to test the ladder only to see if there is a problem from the samples themselves or with the preparation (agarose + buffer TAE 50x+ distilled water) => #Second attempt


#Second attempt

STEP 3.2.1.jpg STEP 3.2.2.jpg STEP 3.2.3.jpg STEP 3.2.4.jpg

=> Same problem : the ladder was growing as one bloc only (see the little drawing). Even during a 2.2 attempt with new SERVA Stain G (which I thought it could be the problem, since the previous tube was quiet old). Then, I noticed that the positive side was turning in blue color and some part of the agarose gel was melting down. So I decided to test if this bleu color is coming from oxidation of the electrodes themselves, or if the ladder was "swimming" on the extra amount of solution (buffer TAE 50x + distilled water) above the agarose to reach the positive side => #Third attempt


#Third attempt

STEP 3.3.1.jpg STEP 3.3.2.jpg

=> Still turning bleu. Even with smaller electrodes that are completely covered by the solution (buffer TAE 50x + distilled water) So I decided to test if this oxidation is coming from the buffer or if it is simply a natural process => #Fourth attempt


#Fourth attempt

STEP 3.4.1.jpg STEP 3.4.2.jpg

=> First picture : distilled water only. Second picture : distilled water + buffer TAE 50x. No changes at all. So it might come from the SERVA Stain G (which is yellow-ish) or it is actually not a problem and does not affect on the electrophoresis itself.