Steps for micropropagation
1. Suitable tissue is selected and cutting is made (explant), usually meristematic tissue as its free from viruses
2. Explant is sterilised using dilute bleach or alcohol (kill any microbes which would thrive in these conditions but not killing sample)
3. Explants placed on sterile growth medium e.g. agar gel containing suitable nutrients (amino acids, glucose, phosphates)
4. High concentration of auxins and cytokinins stimulates explant cell division by mitosis to form callus (totipotent cells)
5. Callus divides to form a larger number of small clumps of undifferentiated cells
6. Clumps stimulated to grow, divide and differentiate. Achieved by moving cells into different growth medium. 100 auxin:1 cytokinin (root formation) 4 auxin:1 cytokinin (shoot formation)
7. After platelets have formed, they are transferred to a greenhouse to be grown in compost of soil and acclimatise to normal growing conditions