NYMU Taipei/Lab Notes/2007 9 16
From 2007.igem.org
< NYMU Taipei/Lab Notes
Revision as of 10:42, 16 September 2007 by Lihsiangyen (Talk | contribs)
Enzyme Digestion
- Enzyme digestion: CinR+HSL (with RBS) with EcoRI, SpeI
- CinR+HSL (1~4): 14ul
- 因為濃度未知, 所以用最大體積
- EcoRI: 1ul (20,000 units/ml)
- SpeI: 1ul (10,000 units/ml)
- 10x EcoRI buffer: 2ul
- Total: 20ul
- CinR+HSL (1~4): 14ul
- Enzyme digestion: D-term with EcoRI
- Original we need double digestion EcoRI and XbaI.
- However, NEB recommend to perform the digestion in sequential manner.
- Thus, we digest the EcoR1 first
- D-term: 11ul (損失因子10, 目標重量300ng)
- 300(ng) * 10 = 3(ug) = 0.27 (ug/uL) * X(uL), X = 3/0.27 = 11.11111111
- EcoRI: 1ul
- 10x EcoRI buffer: 2ul
- H2O: 6ul
- Total: 20ul
Gel separation
- 1% gel, TAE 1X, 30 min, 100v
- 11 lanes (left most is marker)
- each sample (24 uL) are separated into 2 lanes (12 uL for each lane)
- CinR+HSL #1-#4 (lane 2-9) and D-term (lane 10-11)
- use 1Kb ladder
- CinR+HSL insert size = 1.53 Kb
- D-term vector size = 3.284 Kb
- 6X dye
- total volume after digestion is 20uL
- thus, the dye is 4uL
- X/(20+X) = 1/6, X = 4
- sample after dye addition is 20 + 4 = 24 uL