- I swab the laboratory bench with ethanol (70%)
- I cut a small piece of cauliflower – roughly a centimetre across-with a sharp scalpel.
- I place it in a Petri dish using sharp cuts, divide the piece of cauliflower into three.
- I carefully place the pieces of cauliflower, or explants into 50cm3 of sodium hypochlorite solution in a beaker to sterilise them.
- I left it for 10 minutes.
- I undid the ***** cap, then flame the neck of the bottle of the sterile distilled water provided.
- I poured out 50 cm3 of sterile distilled water into three 100 cm3 beakers.
- I flame the neck of the bottle and replace the cap.
- I dipped the end of a pair of forceps into a beaker of ethanol, keeping this well away from the flame.
- I passed the forceps through a blue Bunsen flame to ignite the ethanol and sterilise them.
- I allowed the forceps o cool and then aseptically transfer the explants to a beaker of sterile water. I left it for one minute.
- I rinse the explants twice more in the remaining two beaker of sterile distilled water. This rinsing process is critical to the growth of the explants. I left it in the beaker until required.
- to the hand opposite I wrote with I removed the aluminium foil and cotton wool plug from the test tube of growth medium.
- I flamed the neck of the tube.
- I was using a pair of sterile forceps then I carefully but quickly transfer one of the explants onto the surface of the growth medium in the tube.
- I carefully flame the neck of the tube and replaced the cotton wool.
- I covered the cotton wool with aluminium foil.
- I repeated stage 15 to 17 with the other two explants. I transferred them aseptically to two further tubes of growth media.
- I kept the explants in a warm light place.
- The growth of the explants should be visible after about 10 days.
- In the tube, aseptic technique has not been observed, and the explant has not grown.
- My healthy explants and contaminated explants compared.





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