Team:Stockholm/16 July 2010

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(Difference between revisions)
(New page: {{Stockholm/Top2}} ==Andreas== ===LMWP ligation=== Nina back from vacation and we decided to start working harder on making our CPPs. We divided TAT, Transportan10 and LMWP between us; I...)
(Ligation)
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'''Procedures'''
'''Procedures'''
-
#Denaturation: 95°C, 10 min
+
#'''Denaturation:''' 95°C, 10 min
 +
#Temperature slowly lowered to 65°C
 +
#'''Annealing:''' 65°C, 5 min
 +
#Temperature slowly lowered to RT (≈27°C)
 +
#'''Ligation:''' Quick Ligase added
 +
#*25°C, 10 min
 +
#'''Transformation''': 6 μl ligation mix into Top10. Cells grown on LB agar + 25 μg/ml Cm.

Revision as of 19:29, 29 July 2010


Contents

Andreas

LMWP ligation

Nina back from vacation and we decided to start working harder on making our CPPs. We divided TAT, Transportan10 and LMWP between us; I got LMWP.

LMWP primer dilutions

All LMWP primers were diluted 100x and 1000x, to yield concentrations of ≈1.0 and 0.1 μM, respectively:

Primer Original conc. 100x dil. conc. 1000x dil. conc.
LMWP_C_F1 109 mM 1.09 mM 0.11 mM
LMWP_N_F1 141 mM 1.41 mM 0.14 mM
LMWP_CN_R1 131 mM 1.31 mM 0.13 mM
LMWP_CN_F2 120 mM 1.20 mM 0.12 mM
LMWP_C_R2 119 mM 1.19 mM 0.12 mM
LMWP_N_R2 139 mM 1.39 mM 0.14 mM


Flanking primers are designed with EcoRI and PstI overhangs, allowing me to use the linearized pSB1C3 vector for the ligation reaction.

Ligation

LMWP designed in two versions:

  • C-LMWP containing the standard Freiburg prefix.
  • N-LMWP containing the Freiburg N-part prefix.

Two ligation reactions performed for each LMWP version: (1) with high concentration primers (100x dil.) and (2) with low concentration primers (1000x dil.).

Ligation mixes

Ingredient C-LMWP (high conc.) [μl] N-LMWP (high conc.) [μl] C-LMWP (low conc.) [μl] N-LMWP (low conc.) [μl]
pSB1C3 vector (25 ng/μl) 2 2 2 2
LMWP_C_F1 1 0 1 0
LMWP_CN_R1 1 1 1 1
LMWP_CN_F2 1 1 1 1
LMWP_C_R2 1 0 1 0
LMWP_N_R2 0 1 0 1
2X Quick Ligase buffer 10 10 10 10
dH2O 3 3 3 3
Quick Ligase (added later) 1 1 1 1
Total volume 20 20 20 20

Procedures

  1. Denaturation: 95°C, 10 min
  2. Temperature slowly lowered to 65°C
  3. Annealing: 65°C, 5 min
  4. Temperature slowly lowered to RT (≈27°C)
  5. Ligation: Quick Ligase added
    • 25°C, 10 min
  6. Transformation: 6 μl ligation mix into Top10. Cells grown on LB agar + 25 μg/ml Cm.