Plant Genomic DNA Extraction
Last week friday, we was given a chance on running an experiment- Plant Genomic DNA extraction.... It is very interesting..... and gain a lot of knowledge and skills
Last week friday, we was given a chance on running an experiment- Plant Genomic DNA extraction.... It is very interesting..... and gain a lot of knowledge and skills
Plant Acacia mangium had been used on this experiment. The experiment started by doing some cleaning on the Acacia leaf then followed cut it into small pieces.... ( This methods make it easy for disrupting the cell wall of the leaves)
Later, Liquid Nitrogen is added into the mortal in order to freeze the leaves... then the leaves is rapidly grind into a fine powder with a pestle and mortar as the liquids nitrogen boils off (Liquids nitrogen is added to keep the powder from thawing while grinding)
* Note: Liquids Nitrogen is extremely harmful and extra precaution must be taken
Remember to wear double layer of Gloves...
* Note: Liquids Nitrogen is extremely harmful and extra precaution must be taken
Remember to wear double layer of Gloves...
In order to prevent contamination, all of our experiment is done on the laminar flow hood... Due to laminar flow hood is not enough to provide for all 139 of biotechnology students, so we have to share each others.. Queue up in a line...
This is the sample after CIA solution is added and centrifuge at 13000rpm for 5 minutes to obtain supernatant. The supernatant is carefully transfered into the sterile, new, clean 2.0ml microcentrifuge tube
This is the sample after cold isopropanol is added and centrifuge at 13000 rpm for 2 minutes in order to precipitate nucleic acids. Then after that it is store at -20 degree celcius freezer for at least 30 minutes.
Look!! One of friend is pipetting the supernatant out from the centrifuge tube into a new tubes...
After 30 minutes, centrifugation at 13000 rpm for 2 minutes to obtain the pellet DNA. After the pellet of DNA is obtained, the supernatant is discarded. Then DNA wash buffer is added and rinse the pellet by tapping the tube gently with finger tips ( the dilute ethanol removes salts ).
After that, centrifuge again at 13000rpm for 2 minutes. Supernatant is discarded and let the pellet air dry before resuspend in TE buffer for further analysis.
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