PGLO transformation
![Image](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhabdhKqkFLukdkZnXIHc8s1dEbMShUNhY4jPrHY0HfIiLageF_W4xsJMRB-Mm_xjG7fkq6nbSHUCxEInMglDxw5XTVrSOoh60j5QGh1iQtP-Eg78HoQ5zcwzj0Mj2vsZ18EikqDZDyE5E/s400/IMG_4227.jpg)
PGLO transformation 1. Label two B12 competant (able to take DNA) Ecoli cell tubes and (-) PGLO, (+) PGLO and place on ice. 2. Transfer 250 µm of cold transformation solution CaCl2 into each tube 3. Place tubes on crushed ice 4. Using pipet 10 µL of PGLO plamid (DNA) into + PLGO tube. 5. Incubate tubes onn ice for 10 mins 6. Lable 4 agar plates on the bottom (1) LB with (-) PGLO (2) LB/Amplara with (-) PGLO (3) LB/Amplara (+) PGLO (4) LB/Amplara/Ara (+) PGLO Note: We must test the result that (1) Cell can grow with lots of growth (2) No growth (3) Growth not much (4) Growth/ Glow (Has a light) 7. Heat shock using both for (-) PGLO, (+) PGLO tubes into water bath at 42 degrees celsius for 50 sec. Then place back on ice in 2 mins. 8. Remove from ice and rack. Add 250 µm LB broth into tubes and incubate at room temp for 10 min 9. Grenly flick closed...